Laura Brown
Dr Laura Brown MBA, BSc (Biochemistry), BSc (Psychology), PhD, Diploma in Clinical Science, FICR, is a Pharmaceutical Management and Training Consultant, Course Director for the MSc in Clinical Research at the University of Cardiff, and MSc Regulatory Affairs, TOPRA. She has more than 19 years’ experience in the pharmaceutical industry and has worked for several companies, including GlaxoWellcome, Hoechst Marion Roussel, Farmitalia and Phoenix International. She has worked in Drug Development, Clinical Research, Quality Assurance and Marketing and has a particular expertise in Clinical Research and GCP issues. She was Chairman of the ACRPI GCP Forum for six years. She regularly writes on clinical research issues and ICH GCP, is author of SCRIP’s GCP guide and is a member of the editorial board of the Good Clinical Practice Journal.She is co-author of several books on management including ‘Developing the Individual’,‘The Ultimate Book of Business Skills’ and ‘Pharmaceutical Project Management’.
Clinical Trial Regulatory Requirements
28-29 Jan 2021
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 existing Directive requirements.
Data Integrity and Document Management
5 Mar 2021
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.
Risk Management for Pharma and Biopharma Professionals
22 Mar 2021
This essential course will explain the importance of using risk management techniques in drug and device development to comply with the latest focus on inspection in this area.
GCP and Clinical Research Update - Hot Inspection Topics
23 Mar 2021
This course provides an update on recent changes to ICH GCP R2, EU Clinical Trial Regulation and guidance and will discuss how these changes have been implemented
Leadership Skills for Pharmaceutical Professionals
12-13 Apr 2021
This comprehensive two-day course will introduce you to the core concepts of what makes an excellent leader - in the context of the pharmaceutical industry - and how to apply the different skills of leading your staff and team to maximise results
EU Clinical Trial Regulation: Overview and Implementation
22-23 Apr 2021
This course will provide an essential understanding to help with compliance with the new regulation and associated implementing acts and other texts for carrying out clinical trials in the EU
Managing Vendor/CRO/CMO Oversight
26-27 Apr 2021
Learn how to prepare a Request for Proposal (RFP), evaluate and select the right CRO and establish procedures for vendor oversight for R&D projects you need to outsource
An Essential Overview of the Pharmaceutical and Biotech Industries
7 May 2021
This programme will give you an invaluable overview of the pharmaceutical industry, from discovery of the molecule through development to marketing.
The Pharma Mini MBA
12-14 May 2021
A three-day accelerated management programme to give you the high-performance management skills of an MBA, designed specifically for pharmaceutical/biotechnology professionals and also applicable to medical device/animal health industries
Clinical Quality Management Systems
17-18 May 2021
A two-day course that will ensure you comply with new regulatory requirements.
Project Management for Pharma Professionals
15-16 Jun 2021
The leading project management course designed specifically for the pharma/bio industries – also applicable to those working in medical devices and animal health
*Includes:* Interactive workshop sessions
Project Management for Pharma Professionals
17-18 Jun 2021
The leading project management course designed specifically for the pharma/bio industries – also applicable to those working in medical devices and animal health
*Includes:* Interactive workshop sessions
Strategic Thinking in the Pharma and Biopharma Industry
21-22 Jun 2021
Strategy and strategic thinking skills in a covid-19 environment.
How to Write Effective SOPs
28 Jun 2021
An essential course for ensuring compliance with regulatory requirements which will be of particular relevance for pharmacovigilance, regulatory affairs, clinical research/operations, GMP, QA and document management functions.
CAPA (Corrective and Preventative Action)
29 Jun 2021
This course will cover CAPA methodology and documentation, diagnosing process improvement, developing options for process improvement and CAPA and planning and implementation in practice of improvements and CAPA.
Clinical Trial Regulatory Requirements
5-6 Jul 2021
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 existing Directive requirements.
Critical Thinking for Pharma and Biopharma Professionals
9 Jul 2021
This programme will explore the key concepts of critical thinking applied to problem solving and decision making for pharmaceutical and biopharmaceutical professionals
Project Management for Pharma Professionals
9-10 Sep 2021
The leading project management course designed specifically for the pharma/bio industries – also applicable to those working in medical devices and animal health
*Includes:* Interactive workshop sessions
An Essential Overview of the Pharmaceutical and Biotech Industries
16 Sep 2021
This programme will give you an invaluable overview of the pharmaceutical industry, from discovery of the molecule through development to marketing.
An Essential Overview of the Pharmaceutical and Biotech Industries
17 Sep 2021
This programme will give you an invaluable overview of the pharmaceutical industry, from discovery of the molecule through development to marketing.
Risk Management for Pharma and Biopharma Professionals
21 Sep 2021
This essential course will explain the importance of using risk management techniques in drug and device development to comply with the latest focus on inspection in this area.
GCP and Clinical Research Update - Hot Inspection Topics
22 Sep 2021
This course provides an update on recent changes to ICH GCP R2, EU Clinical Trial Regulation and guidance and will discuss how these changes have been implemented
Risk Management for Pharma and Biopharma Professionals
23 Sep 2021
This essential course will explain the importance of using risk management techniques in drug and device development to comply with the latest focus on inspection in this area.
GCP and Clinical Research Update - Hot Inspection Topics
24 Sep 2021
This course provides an update on recent changes to ICH GCP R2, EU Clinical Trial Regulation and guidance and will discuss how these changes have been implemented
Leadership Skills for Pharmaceutical Professionals
28-29 Sep 2021
This comprehensive two-day course will introduce you to the core concepts of what makes an excellent leader - in the context of the pharmaceutical industry - and how to apply the different skills of leading your staff and team to maximise results
Leadership Skills for Pharmaceutical Professionals
30 Sep-1 Oct 2021
This comprehensive two-day course will introduce you to the core concepts of what makes an excellent leader - in the context of the pharmaceutical industry - and how to apply the different skills of leading your staff and team to maximise results
Data Integrity and Document Management
4 Oct 2021
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.
Data Integrity and Document Management
5 Oct 2021
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.
Managing Vendor/CRO/CMO Oversight
7-8 Oct 2021
Learn how to prepare a Request for Proposal (RFP), evaluate and select the right CRO and establish procedures for vendor oversight for R&D projects you need to outsource
Managing Vendor/CRO/CMO Oversight
11-12 Oct 2021
Learn how to prepare a Request for Proposal (RFP), evaluate and select the right CRO and establish procedures for vendor oversight for R&D projects you need to outsource
Strategic Thinking in the Pharma and Biopharma Industry
14-15 Oct 2021
Strategy and strategic thinking skills in a covid-19 environment.
EU Clinical Trial Regulation: Overview and Implementation
18-19 Oct 2021
This course will provide an essential understanding to help with compliance with the new regulation and associated implementing acts and other texts for carrying out clinical trials in the EU
EU Clinical Trial Regulation: Overview and Implementation
20-21 Oct 2021
This course will provide an essential understanding to help with compliance with the new regulation and associated implementing acts and other texts for carrying out clinical trials in the EU
The Pharma Mini MBA
10-12 Nov 2021
A three-day accelerated management programme to give you the high-performance management skills of an MBA, designed specifically for pharmaceutical/biotechnology professionals and also applicable to medical device/animal health industries
The Pharma Mini MBA
15-17 Nov 2021
A three-day accelerated management programme to give you the high-performance management skills of an MBA, designed specifically for pharmaceutical/biotechnology professionals and also applicable to medical device/animal health industries
Clinical Quality Management Systems
18-19 Nov 2021
A two-day course that will ensure you comply with new regulatory requirements.
Critical Thinking for Pharma and Biopharma Professionals
22 Nov 2021
This programme will explore the key concepts of critical thinking applied to problem solving and decision making for pharmaceutical and biopharmaceutical professionals
Clinical Quality Management Systems
25-26 Nov 2021
A two-day course that will ensure you comply with new regulatory requirements.
How to Write Effective SOPs
2 Dec 2021
An essential course for ensuring compliance with regulatory requirements which will be of particular relevance for pharmacovigilance, regulatory affairs, clinical research/operations, GMP, QA and document management functions.
CAPA (Corrective and Preventative Action)
3 Dec 2021
This course will cover CAPA methodology and documentation, diagnosing process improvement, developing options for process improvement and CAPA and planning and implementation in practice of improvements and CAPA.
How to Write Effective SOPs
6 Dec 2021
An essential course for ensuring compliance with regulatory requirements which will be of particular relevance for pharmacovigilance, regulatory affairs, clinical research/operations, GMP, QA and document management functions.
CAPA (Corrective and Preventative Action)
7 Dec 2021
This course will cover CAPA methodology and documentation, diagnosing process improvement, developing options for process improvement and CAPA and planning and implementation in practice of improvements and CAPA.
Project Management for Pharma Professionals
9-10 Dec 2021
The leading project management course designed specifically for the pharma/bio industries – also applicable to those working in medical devices and animal health
*Includes:* Interactive workshop sessions
Project Management for Pharma Professionals
13-14 Dec 2021
The leading project management course designed specifically for the pharma/bio industries – also applicable to those working in medical devices and animal health
*Includes:* Interactive workshop sessions