Qualified person

Results: 450



#Item
371Pharmacology / Health / Drug safety / Pharmacy / Pharmacovigilance / European Medicines Agency / Directive 2001/83/EC / Qualified Person Responsible For Pharmacovigilance / Qualified Person for Pharmacovigilance / Pharmaceutical sciences / Clinical research / Pharmaceuticals policy

EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 635

Add to Reading List

Source URL: ec.europa.eu

Language: English - Date: 2013-10-30 04:33:16
372Pharmacy / Health / Pharmacovigilance / Pharmaceuticals policy / Clinical research / Qualified Person for Pharmacovigilance / Pharmaceutical sciences / Drug safety / Pharmacology

EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 617

Add to Reading List

Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 08:48:55
373Pharmaceutical sciences / Health / Pharmaceutical industry / European Medicines Agency / Pharmacology / Qualified Person / Supplementary protection certificate / European Directive on Traditional Herbal Medicinal Products / Clinical research / Pharmaceuticals policy / Research

Vet MAA Form published January 2014 updated 30 Jan further to comment received on annex

Add to Reading List

Source URL: ec.europa.eu

Language: English - Date: 2014-01-31 02:57:55
374Medicine / Research / Good Laboratory Practice / Directive 2001/83/EC / Medical device / Cell therapy / Qualified Person / Biologic / Electronic cigarette / Pharmaceuticals policy / Clinical research / Biology

          Consultation Paper 

Add to Reading List

Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:02:34
375Pharmacy / Health / Pharmaceutical industry / Executive agencies of the United Kingdom government / Qualified Person / Good distribution practice / Medical device / Veterinary Medicines Directorate / Directive 2001/83/EC / Pharmaceuticals policy / Clinical research / Medicine

Notes for applicants and holders of a Wholesale Dealer’s Licence (WDA(H)) or Broker Registration MHRA Guidance Note 6 1

Add to Reading List

Source URL: www.mhra.gov.uk

Language: English - Date: 2014-07-03 12:41:38
376Pharmaceutical industry / Clinical research / Health / Good manufacturing practice / European Directive on Traditional Herbal Medicinal Products / Qualified Person / European Medicines Agency / Medical device / EudraLex / Pharmaceuticals policy / Medicine / Pharmaceutical sciences

Notes for applicants and holders of a Manufacturer’s Licence MHRA Guidance Note 5 1

Add to Reading List

Source URL: www.mhra.gov.uk

Language: English - Date: 2014-07-03 12:41:08
377Cefuroxime / Qualified Person Responsible For Pharmacovigilance / Injection / Cephalosporin / Pharmacovigilance / Summary of Product Characteristics / Pharmacology / Pharmaceutical sciences / Chemistry

UKPAR CEFUROXIME 250MG POWDER FOR SOLUTION FOR INJECTION AND CEFUROXIME 1.5G POWDER FOR SOLUTION FOR INJECTION OR INFUSION PL[removed]Cefuroxime 250mg powder for solution for injection

Add to Reading List

Source URL: www.mhra.gov.uk

Language: English - Date: 2014-06-18 05:51:10
378Research / Pharmacology / Pharmaceuticals policy / Pharmaceutical industry / Stem cells / Cell therapy / Medical device / Food and Drug Administration / Qualified Person / Biology / Clinical research / Medicine

ISCT HEAD OFFICE Suite[removed]West 5th Avenue Vancouver, BC Canada V5Y 1J6 Tel: [removed]

Add to Reading List

Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:02:36
379Pharmaceuticals policy / Pharmacology / Clinical research / Pharmaceutical industry / Pharmacy / Qualified Person / Medical device / British Pharmacopoeia / Good manufacturing practice / Medicine / Pharmaceutical sciences / Health

The supply of unlicensed medicinal products (“specials”) MHRA Guidance Note 14 1

Add to Reading List

Source URL: www.mhra.gov.uk

Language: English - Date: 2014-05-06 06:19:28
380Qualified Person for Pharmacovigilance / Health / Medicine / Research / Drug safety / Pharmacology / Pharmacy

Public Consultation Paper Review of Commission Regulation (EC) n° [removed]Final EFPIA/EVM/EBE comments) General comments Company

Add to Reading List

Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:34:54
UPDATE