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Qualified Person Education Course Module A PLUS IMP Pre-Course Session

4-6 June 2024
Munich, Germany

EQPA Members Area

IMP Working Group Members Area

Document and track your personal development - with the Continuous Professional Development (CPD) Documentation Template

To access the template for documenting and tracking your past and ongoing activities, please go here.

After filling out the form, you will be able to create and print out a PDF file.

Membership - Application form
Associate Membership

Here you can apply for associate membership. If you are not sure what status applies to you, please see the information on requirements.

*) Obligatory fields

Personal Information*


	Mr Mx Ms*

	First Name*

	Last Name*

	Company*

	Department

	Street / P.O. Box*

	City*

	Zip Code*

	Country*

	Phone

	Fax

	E-Mail*

I'm currently preparing to become a Qualified Person*

* Please note that in this case your associate membership is limited to one year, but can be renewed for another one year period.

I'm not a Qualified Person

(Please make sure to fill in the following part)

PLEASE READ CAREFULLY. YOU NEED TO PROVIDE THE FOLLOWING DOCUMENTS BEFORE WE CAN PROCESS YOUR APPLICATION AND CONFIRM YOUR MEMBERSHIP:

a copy of your university degrees
a confirmation from your company that you have acquired practical experience over at least two years, in one or more undertakings which are authorized to manufacture medicinal products, in the activities of qualitative analysis of medicinal products, of quantitative analysis of active substances and of the testing and checking necessary to ensure the quality of medicinal products. The duration of practical experience may be reduced by one year where a university course lasts for at least five years and by a year and a half where the course lasts for at least six years.

I fulfil the QP qualification requirements according to the EU Directives and

I’m working in a EU member state, official EU member candidate or proposed candidate, but I’m not (yet) registered, appointed or approved as QP or currently not working as QP

I’m about to assume a similar function (Authorized Person or equal) in a country that has a MRA Agreement with the EU in place (like, e.g., Switzerland)

I have a similar function in a country outside the EU, but which is member of the Pharmaceutical Inspection Co-operation Scheme (PIC/S)

Please also provide the following information (optional):
My fields of interest are:

	EU Regulatory / GMP Requirement
	Marketing Authorisation
	Batch Release
	Supplier Qualification
	Auditing of Suppliers / Contract Manufacturing
	Preparation for Authority Inspection
	Validation
	Personal Training

I'm involved in the following kind of manufacturing (optional)

* I agree that my details from this form will be collected and processed in order to answer my inquiry. This permission may be withdrawn at any time by writing an email to datenschutz@concept-heidelberg.de. Detailed information about our handling of personal data can be found in our privacy policy.