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Training courses & Webinars:
Pharmaceutical
By attending our pharmaceutical training courses you will gain access to industry, academic and regulatory authority experts with a wealth of experience. Our in-person events also provide the opportunity to network and discuss the challenges and developments with our speakers and other like-minded pharmaceutical professionals.
Discovery, development and manufacture of drugs are central to the pharmaceutical industry. Keeping up-to-date with the latest regulations and new discoveries in this fast-paced environment is essential for all professionals working within the industry. Our pharmaceutical training courses have been designed to focus on the latest developments and best practices, presented by industry experts on key topics across the pharmaceutical lifecycle, including clinical, regulatory, manufacturing, GxP, pharmacovigilance, medical writing and biopharma.
Please note: full product details will be shown on our training portal IPI Academy where you can find out more and book
A Practical Guide to Producing and Maintaining the PSMF
13 Feb 2026 - Online webinar
Also on: 16 Sep 2026
This course provides a practical guide to both producing and maintaining the PSMF to ensure compliance and has been fully revised to include the latest updates.
Presented by Graeme Ladds (bio)
A Practical Guide to Writing Risk Management Plans (RMPs)
20 Mar 2026 - Online webinar
Also on: 19 Oct 2026
Understand the relationship between RMPs and safety reviews; PBRERs/DSURs; licence submissions (CTD) and their maintenance.
Presented by Graeme Ladds (bio)
A Practical Introduction to Good Clinical Practice (GCP)
15 Apr 2026 - Online webinar
Also on: 6 Oct 2026
This highly interactive and practical one-day course will introduce you to both the principles of GCP and give you an understanding of how to practically apply it in different settings.
Achieving Publication Success in Scientific Journals
2 Mar 2026 - Online webinar
Also on: 21 Sep 2026
An essential guide to scientific communication covering the essentials of scientific journals, including publishing houses, metrics and their purpose.
Presented by Samaa Al Tabbah (bio)
Additional Risk Minimization Measures (aRMMs) and Their Effectiveness
3 Dec 2025 - Online webinar
Also on: 16 Jun 2026
Delve into the world of additional Risk Minimization Measures (aRMMs) and explore everything from the regulatory framework surrounding aRMMs to their impact on patient safety and healthcare outcomes.
Presented by Graeme Ladds (bio)
Advanced Pharmacovigilance: From Performing Successful Due Diligence to Benefit-Risk Assessments – What to Consider
23-25 Mar 2026 - Online webinar
Also on: 21 Sep 2026
This course will be of maximum benefit to those drug safety professionals who are working both in the clinical and post-marketing safety arena including QA for auditing.
Presented by Graeme Ladds (bio)
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects
11 May 2026 - Online webinar
Also on: 5 Nov 2026
AI and Machine Learning are revolutionising clinical trial data management by enhancing efficiency, streamlining processes, and minimising human error. This course will be of use in both the pharmaceutical and medical device industry.
Presented by Zuzanna Kwade (bio)
AI in Pharmacovigilance
18 May 2026 - Online webinar
Also on: 18 Nov 2026
In this exciting new course, gain an introduction into the transformative impact of artificial intelligence on drug safety and monitoring.
Presented by Graeme Ladds (bio)
An Essential Overview of Medical Information
4 Dec 2025 - Online webinar
Also on: 22 Jun 2026
In this one-day course, understand everything from the role of medical information to the guidelines for medical information and advertising.
Presented by Graeme Ladds (bio)
An Essential Overview of the Pharmaceutical and Biotech Industries
12 Mar 2026 - Online webinar
Also on: 28 Sep 2026
This programme will give you an invaluable overview of the pharmaceutical industry, from discovery of the molecule through development to marketing.
Presented by Laura Brown (bio)
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals
27 Nov 2025 - Online webinar
Also on: 8 May 2026
This course will cover the key regulations used globally in human factors and usability engineering: the specific standards and guidances, methods, and the tools commonly used in medical device development.
Presented by Greg Thay (bio)
An Introduction to Signal Detection
16 Apr 2026 - Online webinar
Also on: 14 Oct 2026
This course provides a foundation in the critical role of signal detection in ensuring the safety and efficacy of medicines.
Presented by Graeme Ladds (bio)
An Introduction to Technology Transfer for Solid Dosage Forms
6 Mar 2026 - Online webinar
Also on: 18 Sep 2026
This course covers technology transfer for solid dosage forms, focusing on best practices, strategies, and real-world challenges through interactive sessions and case studies.
Presented by Laura Buttafoco (bio)
An Overview of Ethical Standards in Clinical Research Publication
13 May 2026 - Online webinar
Also on: 11 Dec 2026
This course will look at ethical research, responsible authorship, and data integrity while addressing conflicts, misconduct, and copyright issues.
Presented by Samaa Al Tabbah (bio)
An Overview of EU and UK Regulatory Affairs
11-12 Feb 2026 - Online webinar
Also on: 21 Sep 2026
This two-day course provides an introduction to pharmaceutical regulatory affairs and the fundamentals of drug development. It is particularly valuable for those who are new to the regulatory function or work in a supporting or interactive role.
Presented by Norah Lightowler (bio)
Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions
10 Jun 2026 - Online webinar
Also on: 9 Dec 2026
This course will allow participants to explore the regulatory landscapes governing AMR, discover innovative solutions and understand the challenges AMR poses across different sectors.
Presented by Linda Oyama (bio)
APIs in Focus: Understanding ICH, GMP and Supply Chain Excellence
29-30 Apr 2026 - Online webinar
Also on: 21 Oct 2026
This course will cover key terminology, the EU and USA regulatory framework, Good Manufacturing Practice (GMP) requirements including controls and validation, and consider Good Distribution Practice (GDP) and how to manage your supply chain.
Presented by Paul Palmer (bio)
Behavioural Risk Management in Clinical Trials
13 Apr 2026 - Online webinar
Also on: 5 Oct 2026
Explore how human behaviour and stakeholder dynamics create hidden risks in clinical trials. Using the CURED framework and interactive learning, participants will learn to identify and manage relational risks that undermine trust and collaboration. The result: stronger teams, better communication, and more resilient project outcomes.
Presented by Roger Joby (bio)
Best Practice for Writing Effective SOPs
4 Dec 2025 - Online webinar
Also on: 26 Mar 2026
An essential course for ensuring compliance with regulatory requirements and including best practice SOP writing using process mapping.
Presented by Laura Brown (bio)
Best Practices for Supplier Qualification in Life Science
6-7 May 2026 - Online webinar
Also on: 12 Nov 2026
Explore the intricacies of Life Science Supplier Qualification through our comprehensive course. Gain expert insights into regulatory compliance, supply chain optimization, and strategic sourcing. Elevate your proficiency in maintaining product integrity with proven industry best practices.
Presented by Mustafa Edik (bio)
Biosimilars
16-17 Mar 2026 - Online webinar
Also on: 22 Sep 2026
A two-day seminar providing an essential overview of biosmilars and how they differ from the original biological product.
Presented by Andrew Willis (bio)
Biotechnology for the Non-Biotechnologist
10-12 Jun 2026 - London
Also on: 30 Nov 2026
An ideal course for non-scientists and scientists who need to understand the basic theory, principles, techniques and potential of biotechnology.
Presented by
Robert Alvarez (bio)
and 6 more leading experts
Building The Business Case For Pharma 4.0
13 Apr 2026 - Online webinar
Also on: 6 Oct 2026
This course will equip you with the tools and insights needed to articulate your vision, secure funding, and pave the way for Pharma 4.0 success.
Presented by Lewis Shipp (bio)
CAPA (Corrective and Preventative Action)
5 Dec 2025 - Online webinar
Also on: 15 Jun 2026
This course will cover CAPA methodology and documentation, diagnosing process improvement, developing options for process improvement, and planning and implementation in process improvements and CAPA.
Presented by Laura Brown (bio)
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products
23-24 Apr 2026 - Online webinar
Also on: 19 Oct 2026
The regulatory requirements for Biological drug products are complex, and pharmaceutical companies are continuously under pressure to ensure regulatory compliance from drug discovery to post-marketing surveillance.
This course has been designed to help you navigate the complex regulatory requirements for biological drugs, including ATMPs. It will clearly depict the differences between small and large molecules and the development approaches which reflect the type of molecule. It will address the key aspects of the CTD, look at the CMC regulatory requirements during different stages of development, and discuss the importance of change control.
Presented by Andrew Willis (bio)
Cleaning Validation - Best Practice in Pharmaceuticals
2-3 Dec 2025 - Online webinar
Also on: 23 Jun 2026
Master the principles of cleaning validation to ensure pharmaceutical manufacturing equipment meets stringent regulatory standards, preventing contamination and safeguarding public health.
Presented by Mustafa Edik (bio)
Clinical & Post-Marketing Safety
11-12 May 2026 - Online webinar
Also on: 16 Nov 2026
This two-day course covers international standards for clinical and post-marketing drug safety, including ICH guidelines, adverse event reporting, signal detection, and risk management strategies.
Presented by Graeme Ladds (bio)
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application
16-17 Mar 2026 - Online webinar
Also on: 30 Sep 2026
This seminar looks at the latest guidance on how to prepare a clinical overview and summary in accordance with regulatory expectations and to comply with the requirements of the Common Technical Document (CTD).
Presented by John Price (bio)
Clinical Quality Management Systems
23-24 Mar 2026 - Online webinar
Also on: 17 Sep 2026
A two-day course that will ensure you comply with new regulatory requirements.
Presented by Laura Brown (bio)
Clinical Research Project Management
29 Apr-1 May 2026 - Online webinar
Also on: 21 Oct 2026
The leading clinical research project management course designed specifically for the pharma/bio industries – also applicable to those working in medical devices and animal health
Presented by Laura Brown (bio)
Clinical Trial Monitoring
29-30 Jun 2026 - Online webinar
Also on: 10 Dec 2026
This course will assure monitors understand the importance of compliance with latest ICH GCP R3 requirements, and how these apply to monitoring clinical trials in the future.
Presented by Laura Brown (bio)
Clinical Trial Regulatory Requirements
2-3 Mar 2026 - Online webinar
Also on: 14 Sep 2026
This course will take you through the key regulatory and guideline requirements for clinical research in Europe, including the new EU Clinical Trial Regulation and a brief review of key FDA requirements.
Presented by Laura Brown (bio)
Cosmetovigilance
18-19 Jun 2026 - Online webinar
Also on: 8 Dec 2026
This course will provide a comprehensive overview of cosmetogivilance in Europe, the USA and the Rest of the World (ROW).
It will provide key guidance for manufacturers and distributors on how to comply with the regulatory requirements, and will be valuable for pharmaceutical and medical device companies looking to access the cosmetic market.
Presented by Graeme Ladds (bio)
Data Integrity and Document Management
11 Dec 2025 - Online webinar
Also on: 22 Jun 2026
Data integrity is a critical issue in document governance and is increasingly becoming a focus for regulatory inspections globally. This course will equip you with the necessary knowledge to identify and avoid potential data integrity issues before auditors do.
Presented by Laura Brown (bio)
Data Integrity Auditor Masterclass
22-23 Apr 2026 - Online webinar
Also on: 14 Oct 2026
During this course, data integrity will be discussed from the perspective of GxP audits, with practical advice for successful data integrity audits given.
Presented by Mustafa Edik (bio)
Dealing With Scientific Journal Reviewers: From Comments to Resubmission
15 Jun 2026 - Online webinar
Also on: 1 Dec 2026
This course covers journal decision types and techniques for responding effectively to reviewers' feedback, as well as strategies for revising and resubmitting manuscripts to enhance publication success.
Presented by Samaa Al Tabbah (bio)
Development of Combination Products: Critical Interactions
9-10 Feb 2026 - Online webinar
Also on: 16 Sep 2026
Linking the technical requirements of device design and pharmaceutical product development.
Using QbD to deliver drug/device combinations.
Presented by Andrew Willis (bio)
Digital CMC
6 May 2026 - Online webinar
Also on: 2 Nov 2026
Through this interactive session, participants will explore the forces driving the shift toward digital transformation, understand the challenges Digital CMC addresses, and learn about its operational and regulatory advantages.
Presented by Lewis Shipp (bio)
Digital CMC: The Key To Realising Pharma 4.0
23 Jun 2026 - Online webinar
Also on: 4 Dec 2026
Whether you’re looking to optimise existing processes or lay groundwork for a digital transformation, the course will teach the tools to leverage Digital CMC as a cornerstone of Pharma 4.0 success.
Presented by Lewis Shipp (bio)
Digital Technology and Personalisation in Patient Support Programmes
6 May 2026 - Online webinar
Also on: 4 Nov 2026
Learn how to build digital technology that is specifically aligned to match with the patient, the clinical study, the disease and the treatment programme.
Presented by Graham Howieson (bio)
Digital Technology Transfers
4 Mar 2026 - Online webinar
Also on: 22 Sep 2026
This course explores how leveraging digital solutions, companies can not only accelerate the transfer of critical knowledge but also foster innovation and gain an edge in increasingly competitive markets.
Presented by Lewis Shipp (bio)
Effective Change Management in Pharma
17 Apr 2026 - Online webinar
Also on: 9 Oct 2026
Master pharmaceutical change control processes in just 1 hour. Learn GxP compliance, change categories, and regulatory requirements for quality professionals.
Presented by Gurpal Singh (bio)
Effective Communication & Negotiation in Technology Transfers
18 May 2026 - Online webinar
Also on: 15 Oct 2026
The ability to create a working relationship with your partners in a technology transfer is normally overlooked. In the current pharmaceutical landscape, gaining trust should never be an after thought.
Presented by Laura Buttafoco (bio)
Effective Deviation Management Systems in Pharma
20 Mar 2026 - Online webinar
Also on: 25 Sep 2026
Master pharmaceutical deviation management in just 1 hour. Learn root cause analysis, CAPA processes, and compliance requirements to ensure product quality and safety.
Presented by Gurpal Singh (bio)
Effective Regulatory Compliance for Storage and Distribution in Pharma Supply Chains
15 May 2026 - Online webinar
Also on: 20 Nov 2026
Master pharmaceutical compliance essentials for storage and distribution. Learn regulatory requirements, best practices, and 3PL supplier optimisation in just 1 hour.
Presented by Gurpal Singh (bio)
Effective Technical Writing & Editing
15 May 2026 - Online webinar
Also on: 18 Nov 2026
Expert advice on how to write and edit scientific and medical texts, technical documents and those documents needed for regulatory submission.
Presented by Barbara Grossman (bio)
Ensuring Clinical Research Quality & Patient Safety
2 Feb 2026 - Online webinar
Also on: 14 Sep 2026
This course covers Good Clinical Practice (GCP) principles, ensuring participants understand the ethical and regulatory foundations of clinical research, including integrity, safety, consent, data management, and compliance.
Presented by Samaa Al Tabbah (bio)
Essential Documentation Skills for Clinical Research Compliance
9 Mar 2026 - Online webinar
Also on: 5 Oct 2026
Documentation is crucial for regulatory compliance, ensuring accuracy and integrity in clinical trials and laboratory work. GDP has evolved over time, guided by ALCOA & ALCOA-plus principles.
Presented by Samaa Al Tabbah (bio)
EU Pharmaceutical Regulations and Strategy
2-3 Mar 2026 - Online webinar
Also on: 5 Oct 2026
The course will provide an up-to-date overview of the current European pharmaceutical regulatory environment including procedures for obtaining marketing authorisation and post-approval obligations. The proposed changes to the EU pharmaceuticals legislation will be discussed in the relevant sections and impact on strategic considerations for obtaining and maintaining marketing authorisations Procedures for obtaining marketing authorisations in in the UK will be discussed.
Presented by Norah Lightowler (bio)
EU Proposed Pharmaceutical Legislation Changes
19 Jan 2026 - Online webinar
Also on: 1 Jul 2026
This course will provide an up-to-date overview of current European pharmaceutical legislation and the regulatory impact of the proposed changes.
Presented by Norah Lightowler (bio)
GCP and Clinical Research Update - Hot Inspection Topics
19 May 2026 - Online webinar
Also on: 20 Nov 2026
This course provides the latest updates on the finalised ICH GCP E6 R3 guideline, EU Clinical Trial Regulation update, other EU and FDA requirements, consideration for managing studies in the future and AI and other technology developments.
Presented by Laura Brown (bio)
GMP Principles in Vaccine Manufacturing
10-11 Dec 2025 - Online webinar
Also on: 16 Jun 2026
Vaccinology continues to advance and mature impressively, both in developing new and improved vaccines and in administering vaccines to prevent disease. On this course, explore GMP principles in vaccine manufacturing.
Presented by Mustafa Edik (bio)
Golden Rules of Being a Successful GMP Auditor
5-6 Feb 2026 - Online webinar
Also on: 30 Sep 2026
Learn to conduct thorough audits, identify non-conformities, and recommend corrective actions while following the Golden Rules of successful GMP auditing.
Presented by Mustafa Edik (bio)
Good Distribution Practices of Pharmaceuticals and APIs
14-15 May 2026 - Online webinar
Also on: 16 Nov 2026
Gain a comprehensive understanding of industry-leading practices, ensuring precision in distribution from manufacturer to end user. Navigate complex supply chains, focus on compliance, and elevate your commitment to quality assurance throughout the entire distribution process.
Presented by Mustafa Edik (bio)
Good Writing Practice for Clinical Research: Ethics, Standards & Compliance
20 Apr 2026 - Online webinar
Also on: 18 Nov 2026
This course covers ethical standards, data integrity, audience tailoring, document structure, clarity, consistency, citation, and tools for quality control and compliance.
Presented by Samaa Al Tabbah (bio)
How to Audit Pharmaceutical Suppliers (Material and Service)
26-27 Feb 2026 - Online webinar
Also on: 14 Sep 2026
This training provides knowledge and practical skills to effectively audit material and service providers, covering key areas including raw materials, contract manufacturing, logistics, and packaging.
Presented by Mustafa Edik (bio)
How to Deal with Difficult Situations in GMP Audits
5 Mar 2026 - Online webinar
Also on: 28 Sep 2026
This training equips auditors with strategies to handle obstacles such as documentation errors, unethical behaviours, resistance, and time-wasting tactics, ensuring a smooth and productive audit process.
Presented by Mustafa Edik (bio)
How to Interview During GMP Audits
12 Mar 2026 - Online webinar
Also on: 24 Sep 2026
One of the most valuable tools for auditors in the pharmaceutical industry is the ability to conduct thorough and effective interviews during audits. This training will equip you with these essential skills.
Presented by Mustafa Edik (bio)
How to Manage Internal GMP Audits
24-25 Feb 2026 - Online webinar
Also on: 21 Sep 2026
This training programme provides essential skills for planning, managing, and executing internal Good Manufacturing Practices (GMP) audits.
Presented by Mustafa Edik (bio)
How to Pass International Health Authority Inspections
16-17 Apr 2026 - Online webinar
Also on: 7 Oct 2026
This training course prepares professionals in pharmaceuticals, healthcare, and manufacturing to navigate regulatory inspections by major health authorities including the FDA, MHRA, WHO, and EMA.
Presented by Mustafa Edik (bio)
How to Perform Bullet-Proof Good Distribution Practices (GDP) and Good Storage Practices (GSP) Audits
18-19 Jun 2026 - Online webinar
Also on: 10 Dec 2026
This training will equip attendees with the practical skills necessary to implement regulatory-compliant distribution and storage systems, ensuring both pharmaceutical integrity and patient safety.
Presented by Mustafa Edik (bio)
Literature Searching in Drug Safety
14-15 May 2026 - Online webinar
Also on: 10 Nov 2026
This two-day course offers a thorough understanding of literature searching in drug safety, covering regulatory requirements, search criteria, and the interpretation of safety data, while also providing practical assessments to apply knowledge to real-world pharmacovigilance cases.
Presented by Graeme Ladds (bio)
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3
13-14 Apr 2026 - Online webinar
Also on: 15 Oct 2026
Optimising oversight for inspection compliance.
Presented by Laura Brown (bio)
Mastering CTD Submissions in the MENA Region
19 May 2026 - Online webinar
Also on: 26 Nov 2026
This one-day course will provide you with an in depth understanding of the technical and regulatory requirements of CTD submissions in different countries in the MENA region.
Presented by Mohammad Fat'hy Elnadi (bio)
Mastering Ethical and Effective Scientific Publishing: Applying Good Publication Practice (GPP)
20 Jan 2026 - Online webinar
Also on: 8 Jul 2026
This course equips attendees with practical strategies to enhance the clarity, impact, and ethical compliance of their publications.
Presented by Samaa Al Tabbah (bio)
Mastering Grant Writing: Essential Skills for Crafting Winning Proposals
22-23 Jun 2026 - Online webinar
Also on: 8 Dec 2026
This course provides a comprehensive guide to grant writing, covering funder identification, proposal development, submission strategies, post-submission processes, partnerships, technology use, and ethical considerations.
Presented by Samaa Al Tabbah (bio)
Measuring Performance in Clinical Research Management
6 May 2026 - Online webinar
Also on: 23 Nov 2026
This workshop will focus on the effective use of metrics to monitor the real progress of your clinical research project. A valuable master class for anyone involved in clinical research.
Presented by Roger Joby (bio)
Medical Editing for Peer-Reviewed Journals
8 May 2026 - Online webinar
Also on: 4 Nov 2026
This course will provide attendees with fundamental editing skills, enabling them to refine their own research articles or edit the work of other researchers with confidence.
Presented by Alex Evans (bio)
Medical Writing Excellence: Crafting Compelling Scientific Documents
4-5 Feb 2026 - Online webinar
Also on: 30 Sep 2026
Explore the fundamental rules of scientific writing, learning how to organise and present complex research in a clear, ethical and compelling manner.
Presented by Samaa Al Tabbah (bio)
Medical Writing for Consumers
21 Apr 2026 - Online webinar
Also on: 1 Oct 2026
On this course, learn the basics of writing health and medical articles for the consumer.
Presented by Alex Evans (bio)
Medical Writing with AI
18 Jun 2026 - Online webinar
Also on: 8 Dec 2026
Explore the intersection between AI and medical communications in this medical writing power hour.
Presented by Alex Evans (bio)
Microbiomics in Clinical Trials
26 Feb 2026 - Online webinar
Also on: 14 Sep 2026
Explore the microbiome and its high clinical relevance, as well as learning about the different methodology used in microbiomic clinical trials.
Presented by Nikolaj Sørensen (bio)
Molecular Biology for the Non-Molecular Biologist
20-21 Apr 2026 - Online webinar
Also on: 8 Oct 2026
Explore the applications and significance of molecular biology in the pharmaceutical industry, covering DNA, RNA, proteins, gene expression, biotechnology, drug discovery, personalised medicine, and the latest breakthroughs like CRISPR-Cas9 and mRNA vaccines.
Presented by Sayed Goda (bio)
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products
2-3 Mar 2026 - Online webinar
Also on: 14 Sep 2026
Gain practical guidance on EU and FDA regulations for drug/device combination products, along with solutions to current challenges, in this comprehensive course.
Presented by
Tina Amini (bio)
and 3 more leading experts
Navigating ICH GCP E6 (R3): What You Need to Know
29 Jan 2026 - Online webinar
Also on: 13 Jul 2026
This brand new course on the recently published and long-awaited ICH GCP E6 (R3) is designed to help participants stay compliant and implement the new guideline effectively.
Presented by Laura Brown (bio)
New EU GMP Annex 1: Compliant Sterile Medicinal Products
19-21 May 2026 - Online webinar
Also on: 24 Nov 2026
Maintaining a sterile production environment on an ongoing basis is critical in the production of sterile pharmaceuticals, and strict adherence to guidelines and relevant standards is required to minimize contamination risks and ensure product quality and safety.
During this training, all changes in Annex 1 will be evaluated, and the minimum requirements that aseptic operations must meet will be discussed and presented to the participants through examples.
Presented by Mustafa Edik (bio)
Orphan Drug Regulatory Masterclass: EU & US Insights
4 Mar 2026 - Online webinar
Also on: 6 Oct 2026
This must-attend event will provide an essential overview of the opportunities and challenges presented by orphan drug regulation.
Presented by Shaun Stapleton (bio)
Pharmaceutical Development of ATMPs
18-19 Mar 2026 - Online webinar
Also on: 28 Sep 2026
This course will provide a comprehensive overview of the regulatory, quality and GMP requirements to consider when developing ATMPs.
Presented by Andrew Willis (bio)
Pharmaceutical Packaging Essentials: From Regulatory Compliance to Market Success
26-28 Jan 2026 - Online webinar
Also on: 6 Jul 2026
Master pharmaceutical packaging essentials in 3 days: materials selection, regulatory compliance, and testing requirements. Led by industry expert with 25+ years' experience.
Presented by Chris Penfold (bio)
Pharmaceutical Regulatory Affairs in Africa
6-7 May 2026 - Online webinar
Also on: 3 Nov 2026
Covering the key regions of South Africa, Namibia, Zimbabwe, Zambia, Malawi, Tanzania, Kenya, Uganda, Nigeria, Ghana and Maghreb countries - Algeria, Morocco, Tunisia
Pharmaceutical Regulatory Affairs in Asia
24-26 Mar 2026 - Online webinar
Also on: 20 Oct 2026
This seminar will provide an overview of the key areas of pharmaceutical regulatory affairs in Asia including, China, Hong Kong SAR, Brunei, the Philippines, India, Indonesia, Malaysia, Singapore, Thailand, Cambodia, Laos, Vietnam, Taiwan, Korea, Japan
Pharmaceutical Regulatory Affairs in China
3-4 Jun 2026 - Online webinar
Also on: 25 Nov 2026
A detailed overview of the key areas of pharmaceutical regulatory affairs in China, Hong Kong, Macau and Taiwan.
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union
5-6 Mar 2026 - Online webinar
Also on: 30 Sep 2026
This interactive course will discuss the regulatory requirements for human pharmaceuticals within these regions, and discuss the implications of the new joint Eurasian Union regulation.
Presented by Anna Harrington-Morozova (bio)
Pharmaceutical Regulatory Affairs in the Middle East
24-25 Feb 2026 - Online webinar
Also on: 20 Oct 2026
Covering Bahrain, Egypt, Iran, Iraq, Israel, Jordan, Kuwait, Lebanon, Libya, Oman, Palestine, Qatar, Saudi Arabia, Sudan, Syria, UAE and Yemen
Pharmaceutical Regulatory Affairs in the Middle East and North Africa
2-4 Jun 2026 - Online webinar
Covering Bahrain, Egypt, Iran, Iraq, Israel, Jordan, Kuwait, Lebanon, Libya, Oman, Palestine, Qatar, Saudi Arabia, Sudan, Syria, UAE, Yemen, Tunisia, Morocco and Algeria.
Pharmacovigilance Aspects of Licensing Agreements
1-2 Dec 2025 - Online webinar
Also on: 25 Jun 2026
This programme will be of interest to all personnel involved in business development and licensing agreements aspects of pharmacovigilance
Pharmacovigilance QMS & Inspection Preparation
27-28 Apr 2026 - Online webinar
Also on: 8 Oct 2026
This course is designed to help understand pharmacovigilance quality management systems (QMS) and risk-based audits.
Presented by Graeme Ladds (bio)
Pharmacovigilance: An Overview of Drug Safety from Safety Collection to Regulatory Inspection
30 Apr 2026 - Online webinar
Also on: 5 Oct 2026
A practical guide to understanding the role of pharmacovigilance.
Presented by Graeme Ladds (bio)
Practical Requirements of the Arab Pharmacovigilance Guidelines
21-22 Apr 2026 - Online webinar
Also on: 21 Oct 2026
Practical guidance on how to comply with the pharmacovigilance requirements in the Middle East
Presented by Graeme Ladds (bio)
Protein Engineering for Pharmaceutical Biotechnology
21-22 Jan 2026 - Online webinar
Also on: 7 Jul 2026
Advance your expertise in protein engineering with this comprehensive course. Learn cutting-edge techniques in therapeutic development, biotechnology applications, and regulatory compliance, ideal for professionals in pharmaceutical and industrial sectors.
Presented by Sayed Goda (bio)
Real World Evidence (RWE), Real World Data (RWD) and the Application of Artificial Intelligence (AI) in Pharma
22 Jun 2026 - Online webinar
Also on: 2 Dec 2026
A deep dive into the importance of real world evidence (RWE), real world data (RWD) and artificial intelligence (AI) in pharmaceuticals.
Presented by Graham Howieson (bio)
Risk Evaluation and Mitigation Strategies (REMS) vs Risk Management Plans (RMP)
12 Feb 2026 - Online webinar
Also on: 14 Sep 2026
A comprehensive comparison between the importance Risk Evaluation and Mitigation Strategies (REMS) and Risk Management Plans (RMP) in drug safety.
Presented by Graeme Ladds (bio)
Selecting the Best Scientific Journal for Your Research
13 Apr 2026 - Online webinar
Also on: 19 Oct 2026
This session provides an essential guide to selecting both the best and authentic scientific journal for your research, offering practical strategies for using indexing systems and selector tools to enhance visibility and credibility.
Presented by Samaa Al Tabbah (bio)
Signal Detection and Regulatory Expectations
2-3 Feb 2026 - Online webinar
Also on: 30 Sep 2026
This two-day programme will give you a comprehensive review of signal detection and regulatory expectations including the new updated Signal Module IX and Eudravigilance quantitative signal requirement.
Presented by Graeme Ladds (bio)
Signal Detection: A Comprehensive Introduction
28 Jan 2026 - Online webinar
Also on: 1 Jul 2026
A comprehensive introductory guide to signal detection in pharmacovigilance, covering its history, regulations, processes, and safety assessments.
Presented by Graeme Ladds (bio)
Smart Packaging and Electronic Patient Information
15 May 2026 - Online webinar
Also on: 2 Nov 2026
This course will provide an overview of the current technologies, the patient and societal benefits and some building blocks for the establishment and delivery of e-PIL and SMART strategic initiatives.
Presented by Graham Howieson (bio)
Software Automation in Research and Development (R&D) Clinical Trials
17 Mar 2026 - Online webinar
Also on: 28 Sep 2026
This course will help delegates gain a better understanding of the software automation technology driving change within the clinical trials landscape.
Presented by Graham Howieson (bio)
Stability Testing of Pharmaceuticals and Biopharmaceuticals
20-21 May 2026 - Online webinar
Also on: 9 Nov 2026
Design efficient stability studies that are suitable for global marketing. Be able to carry out appropriate stability studies and manage stability samples and facilities, learn how to save resources on stability testing and improve the likelihood of regulatory approval of stability protocols.
Presented by Paul Palmer (bio)
Successful Cognitive Testing in Clinical Drug Trials: Biomarkers, Test Selection & Integration
16 Mar 2026 - Online webinar
Also on: 18 Sep 2026
An excellent opportunity to hear from two renowned cognition experts and gain a better understanding on the selection and successful integration of cognitive testing into therapeutic development programmes, as well as the emerging science of blood-based biomarkers.
Successful Medical Writing – from Protocol to CTD
23-24 Mar 2026 - Online webinar
Also on: 22 Sep 2026
Success in the pharmaceutical industry depends on the speed and efficiency of new drug approvals and the quality of documentation submitted to the regulatory authorities. This intensive, practical medical writing course will benefit participants by enabling them to achieve this standard.
Presented by Cheryl Roberts (bio)
The 2024 EU AI Act
23 Jun 2026 - Online webinar
Also on: 3 Dec 2026
This session will summarise the EU AI Act and its implications on the healthcare sector, including how to be compliant with the new regulatory framework.
Presented by Cheryl Barton (bio)
The Applications of Nanoparticles in the Pharmaceutical and Biomedical Industries
11-12 Mar 2026 - Online webinar
Also on: 15 Sep 2026
Attendees will gain a comprehensive understanding of the science behind nanoparticles, their diverse applications, manufacturing and the opportunities and challenges involved in bringing nanoparticle-based solutions to market.
Presented by Mohammed Alkattan (bio)
The Common Technical Document
24-25 Nov 2025 - Online webinar
Also on: 27 Jan 2026
A comprehensive review of the regulations and technical requirements for chemistry, manufacturing and control (CMC) management of your application.
Presented by Andrew Willis (bio)
The FDA Drug Approval Process
23-24 Feb 2026 - Online webinar
Also on: 24 Sep 2026
A comprehensive overview of FDA procedures, requirements for marketing authorisations and recent developments affecting the drug approval process in the US
Presented by Andrew Willis (bio)
The Principles & Applications of CRISPR
23 Jan 2026 - Online webinar
Also on: 7 Jul 2026
Master CRISPR genome editing fundamentals and real-world applications in medicine, research, and biotechnology with expert-led training and certification.
Presented by Sayed Goda (bio)
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry
20-21 Apr 2026 - Online webinar
Also on: 12 Oct 2026
In this webinar, we will discuss the major requirements and strategies for nitrosamines, a hot topic that is on the forefront of many company's minds.
Presented by Jason Brown (bio)
Thinking Outside of the GMP Box
3-4 Feb 2026 - Online webinar
Also on: 16 Sep 2026
In this two-day course, you will be able to gain a whole new perspective on GMP requirements, including how to implement them.
Presented by Mustafa Edik (bio)
Understanding Computer System Validation (CSV)
24-25 Nov 2025 - Online webinar
Also on: 17 Jun 2026
This course covers the key concepts of computer systems validation and provides practical guidance on how to comply with the regulations applicable to the pharmaceutical industry.
Understanding Scientific Journal Submission and Publication
11 May 2026 - Online webinar
Also on: 16 Nov 2026
This course provides an overview of journal submission, including the types and steps of submissions, as well as effective pre- and post-submission communication to help participants navigate publication successfully.
Presented by Samaa Al Tabbah (bio)
Understanding Toxicology: A Guide for Non-Toxicologists
19 Jan 2026 - Online webinar
Also on: 15 Jul 2026
This introductory course provides a clear and practical foundation in toxicology. It covers key principles, terminology and testing methods, helping participants confidently interpret and apply toxicological data in chemical safety and compliance contexts.
Presented by Laura Robinson (bio)
Upstream and Downstream Manufacturing in the Biopharmaceutical Industry
11 Jun 2026 - Online webinar
Also on: 18 Nov 2026
In this talk, explore the fundamental concepts, techniques, and processes that make up the backbone of biomanufacturing, pharmaceutical production, and biotechnology.
Presented by Mustafa Edik (bio)
US FDA - Understanding Key Factors When Working with the FDA
26 Nov 2025 - Online webinar
Also on: 12 May 2026
This course has been designed to provide an essential overview of the critical factors when working with the FDA (Food and Drug Administration). For those short on time this course is for you, as you will receive a focused and comprehensive overview of the key strategic considerations when making applications to the FDA.
Presented by Andrew Willis (bio)
Utilising Patient Adherence Data and Digital Tools to Improve Patient Outcomes
16 Apr 2026 - Online webinar
Also on: 13 Oct 2026
In this course, you will see the value of remote patient adherence monitoring and learn how to stay ahead of the curve by creating your own digital solutions.
Presented by Graham Howieson (bio)
Variations to Marketing Authorisations
2-3 Jun 2026 - Online webinar
Also on: 11 Nov 2026
A two-day event that will provide an invaluable overview of the EU system for variations, with practical advice on the preparation and submission of variation applications using the various European procedures.
Presented by Andrew Willis (bio)