Animal Health
Biotech
GMP
Intellectual Property
Legal
Management Skills
Medical Devices
Pharma online
Pharmaceutical
Support Staff

Sponsoring & Exhibiting

For sponsorship and exhibition opportunities at Management Forum events click here

Event Management

To find out about event management click here

Speaking Opportunities

Speaking opportunities are available on selected Management Forum events, please contact us for further information

Management Forum Brochure

Download our catalogue here

Medical Devices

28 courses in this category:

9-10 Oct 2018

Medical Device Regulation in the Eurasion Union, Russia and the CIS

A comprehensive overview of medical device regulatory affairs in Russia and the Eurasian Union. Key countries covered include Armenia, Azerbaijan, Belarus, Georgia, Kazakhstan, Kyrgyzstan, Moldova, Russia, Tajikistan, Turkmenistan and Ukraine.

Full details

23 Nov 2017
EUR 979.00
GBP 699.00
USD 1090.00

Also held on:
3 May 2018

An Essential Overview of the Medical Device Industry

This one day workshop aims to give all the key information necessary to understand the regulation of Medical Devices and Diagnostics and to appreciate the key differences from Pharmaceutical regulation.

Full details

20-22 Nov 2017
EUR 2589.00
GBP 1849.00
USD 2884.00

Also held on:
14 May 2018

An Introduction to the Medical Device Regulation

This seminar provides a detailed introduction to the European medical device legislation. It will explain the Regulation and which products are covered, the involvement of Notified Bodies, how to choose one and outline what a manufacturer must do.

Full details

Connectivity in Medical Technology

Understanding connected medical devices, medical mobile Apps and the Medical Device Internet of Things

Full details

9-10 Nov 2017
EUR 2099.00
GBP 1499.00
USD 2338.00

Also held on:
19 Apr 2018

Drug/Device and Device/Drug Combinations in the EU and USA

Practical Guidance on Borderline Issues and Combination Products practical guidance on Borderline issues and combination products

Full details

Dry Powder Inhalers: Annual Conference

Dry Powder Inhalers, Key annual conference for Pharmaceutical and Medical Device Professionals in the DPI market.

Full details

30-31 Jan 2018
EUR 2099.00
GBP 1499.00
USD 2338.00

EC Medical Devices Vigilance System and Post Marketing Surveillance

This conference provides a unique opportunity to meet Competent Authorities, Notified Bodies, Lawyers, consultants and manufacturers to understand and discuss the regulatory and legal requirements with respect to Post Marketing Surveillanc including Vigilance

Full details

28 Feb 2018
EUR 979.00
GBP 699.00
USD 1090.00

Also held on:
21 Sep 2018

Effective Technical Writing & Editing

Expert advice on how to write and edit scientific and medical texts, technical documents and those documents needed for regulatory submission

Full details

7-8 Nov 2017
EUR 2099.00
GBP 1499.00
USD 2338.00

Also held on:
17 Apr 2018

FDA Approval Process for Medical Devices

This seminar will provide a solid foundation in the approval and clearance processes for medical devices in the United States including the underlying legal and regulatory requirements and the ‘general controls’ applicable to all devices.

Full details

6 Dec 2017
EUR 979.00
GBP 699.00
USD 1090.00

Also held on:
28 Jun 2018

How to Write Effective SOPs

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

Full details

27 Feb 2018
EUR 979.00
GBP 699.00
USD 1090.00

Human Factors and Usability Engineering in the Development of Drug Delivery Products

This one-day workshop has been designed specifically for product developers who want to incorporate human factors testing into their product development, or need to provide the regulators with specific usability data for their device

Full details

7 Dec 2017
EUR 979.00
GBP 699.00
USD 1090.00

Also held on:
29 Jun 2018

Improving Processes and CAPA (Corrective and Preventative Action)

This meeting 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

Full details

13-14 Nov 2017
EUR 2099.00
GBP 1499.00
USD 2338.00

Inhaled Drug Delivery

This annual conference will include case studies, regulatory updates, latest therapies and technology innovations in two information pack days

Full details

22-23 Mar 2018
EUR 2099.00
GBP 1499.00
USD 2339.00

Injectable Drug Delivery

The essential conference for pharmaceutical and medical device professionals covering advances in technology for pens, auto-injectors, large volume pumps, patch pumps, needle-free, pre-filled syringes and other parenteral methods – plus a regulatory update

Full details

20-21 Feb 2018
EUR 2099.00
GBP 1499.00
USD 2338.00

Also held on:
19 Sep 2018

ISO 13485: Quality Management Systems for Medical Devices

Compare the requirements of ISO 13485 and ISO 9001, understand the role and responsibilities of quality management. Consider the relationship between ISO 13485 and ISO 14971, Application to Risk Management to Medical Devices

Full details

20-21 Mar 2018
EUR 2099.00
GBP 1499.00
USD 2339.00

Also held on:
4 Oct 2018

Managing Vendor/CRO/CMO Oversight in the Pharma Industry

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.

Full details

Medical Device Regulations in Asia-Pacific Markets

Medical Device Regulations in Asia-Pacific markets, gain practical advice on how regulations are being applied to enable you to maximise on this rapidly growing market.

Full details

Medical Device Regulations in the Middle East

This seminar will provide an essential overview of the key areas of requirements for product approvals for medical devices in the Middle East.

Full details

28-29 Nov 2017
EUR 2099.00
GBP 1499.00
USD 2338.00

Also held on:
29 May 2018

Medical Device Software: Complying with the MDR & FDA Regulations

An Introduction to Medical Device Software: Regulations & Requirements to include EU & FDA Guidance and Risk Management

Full details

29-30 Nov 2017
EUR 2099.00
GBP 1499.00
USD 2338.00

Also held on:
16 May 2018

Medical Device Studies: Clinical Evidence

This seminar has been designed specifically for those who are involved in gathering clinical evidence required for medical devices and in-vitro diagnostic products.

Full details

13 Apr 2018
EUR 979.00
GBP 699.00
USD 1090.00

Also held on:
12 Oct 2018

Medical Device Studies: Regulatory Requirements and Adverse Event Reporting

An essential overview of medical device clinical evaluations, clinical investigations, post-market clinical follow up requirements and adverse event and vigilance reporting

Full details

12-13 Apr 2018
EUR 2099.00
GBP 1499.00
USD 2338.00

Nasal Drug Delivery

This conference gives a comprehensive review within the field of nasal drug delivery while reviewing interesting new data and innovative technologies.

Full details

26-27 Feb 2018
EUR 2099.00
GBP 1499.00
USD 2338.00

Also held on:
25 Sep 2018

New Medical Device Regulation

Managing the transition to the new regulation. This is a seminar you cannot afford to miss
as you put in place your strategies for the new environment.

Full details

26-27 Apr 2018
EUR 2099.00
GBP 1499.00
USD 2338.00

Pharmaceutical Development of ATMPs

This course will provide a comprehensive overview of the regulatory, quality and GMP requirements to consider when developing ATMPs

Full details

21 Mar 2018
EUR 979.00
GBP 699.00
USD 1090.00

Pre-Filled Syringes

Advances in technology for pens, auto-injectors, large volume pumps, patch pumps, needle-free, pre-filled syringes and other parenteral methods plus a regulatory update

Full details

15-17 May 2018
EUR 2589.00
GBP 1849.00
USD 2884.00

Also held on:
15 Oct 2018

Successful Medical Writing

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.

Full details

2-6 Jul 2018
EUR 4199.00
GBP 2999.00
USD 4678.00

The Medical Device Summer School - From Concept to CE Marking

This comprehensive course has been designed to map the processes from device concept to marketing and show how regulatory, quality, clinical and other aspects of device development are joined into a continuous process.

Full details

Wearable Drug Delivery

Technology advances in insulin pumps, transdermal patches, micro needle patches and patch pumps

Full details