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Law and Administration
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Analysis and testing
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Active Substances and excipients
Investigational medicinal products
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Contact
The QP's Notebook
Home
Why
CV
All The Guidance
Study Guide
A - Pharmaceutical law and administration
B - The role and professional duties of a Qualified Person
C - Pharmaceutical Quality Systems
D - Maths and Stats
E - Medicinal chemistry and therapeutics
F - Pharmaceutical formulation and processing
G - Pharmaceutical microbiology
H - Analysis and testing
I - Pharmaceutical packaging
J - Active Substances and Excipients
K - Investigational medicinal products
Question Bank
Scenario Questions
QP Roles and Duties
Law and Administration
Pharmaceutical Quality Systems
Maths and Stats
Medicinal chemistry and therapeutics
Pharmaceutical formulation and processing
Pharmaceutical microbiology
Analysis and testing
Pharmaceutical packaging
Active Substances and excipients
Investigational medicinal products
Training Notes
Thoughts
Contact
Home
Why
CV
All The Guidance
Folder: Study Guide
Back
A - Pharmaceutical law and administration
B - The role and professional duties of a Qualified Person
C - Pharmaceutical Quality Systems
D - Maths and Stats
E - Medicinal chemistry and therapeutics
F - Pharmaceutical formulation and processing
G - Pharmaceutical microbiology
H - Analysis and testing
I - Pharmaceutical packaging
J - Active Substances and Excipients
K - Investigational medicinal products
Folder: Question Bank
Back
Scenario Questions
QP Roles and Duties
Law and Administration
Pharmaceutical Quality Systems
Maths and Stats
Medicinal chemistry and therapeutics
Pharmaceutical formulation and processing
Pharmaceutical microbiology
Analysis and testing
Pharmaceutical packaging
Active Substances and excipients
Investigational medicinal products
Training Notes
Thoughts
Contact

Guidance related to Radiopharmaceuticals

EU Guidance.

 

11. Guideline on good agricultural and collection practice (GACP) for starting materials of herbal origin EMEA/HMPC/246816/2005

Concept paper on the revision of the Guideline on Radiopharmaceuticals - Revision 1

Eudralex - Volume 4 Good manufacturing practice (GMP) Guidelines, Annex 3: Manufacture of Radiopharmaceuticals

EDQM - Guide for the elaboration of monographs on radiopharmaceutical preparations, (2018)

EANM guideline on the validation of analytical methods for radiopharmaceuticals

Draft - Guideline on the non-clinical requirements for radiopharmaceuticals

PIC/S

Guide to Good Manufacturing Practice for Medicinal Products - Annexes - Specifically Annex 3 - Manufacture of radiopharmaceuticals

PIC/S GUIDE TO GOOD PRACTICES FOR THE PREPARATION OF MEDICINAL PRODUCTS IN HEALTHCARE ESTABLISHMENTS - Specifically Annex 3 - Good practices for the preparation of radiopharmaceuticals in healthcare establishments

WHO / IAEA

International Atomic Energy Agency and World Health Organization guideline on good manufacturing practices for radiopharmaceutical products

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