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Current Events

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

26-28 April 2023
Hamburg, 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
Regular Membership

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

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Personal Information*

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  First Name*
  Last Name*
  Company*
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  Street / P.O. Box*
  City*
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I'm a Qualified Person (or equivalent) and registered at the following authority (no company address!):

Authority Name*

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City*

Zip Code*

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I've been registered since*     

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)
Sterile / Aseptic Production (Injectables & others)
Solid Dosage Forms
Semi Solid Dosage Forms
Liquid Non Sterile Dosage Forms
API Production requiring QP release*)
Biologics (Blood, Vaccines...)
Herbals
Investigational Medicinal Products
Advanced therapies (stem cell production etc)
Others (please specify): 
*) Biotech API production (genetic engineering or fermentation) and API production from human or animal sources requires QP release in some European Countries
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