HMA

Results: 2302



#Item
111South African law

CMDh QUESTIONS & ANSWERS CMDh REFERRALS Doc. Ref.: CMDh, RevFebruarySCOPE OF THE PROCEDURE .......................................................................................................

Add to Reading List

Source URL: www.hma.eu

Language: English - Date: 2016-03-04 10:07:02
    112Pharmaceuticals policy / Pharmaceutical industry / Marketing authorization / Pharmacology / Pharmaceutical sciences / Patent application / Health policy

    GUI-010 Duplicate applications in MRP-DCPEMA-CMDv

    Add to Reading List

    Source URL: www.hma.eu

    Language: English - Date: 2015-06-15 05:38:48
    113

    CMDh-IP Meeting on DCP/MRP Improvements| London| 18 MaySplit Procedures An OTC industry perspective Dr Mark B Griffiths (Pfizer Consumer Healthcare)

    Add to Reading List

    Source URL: www.hma.eu

    Language: English - Date: 2015-05-29 10:17:01
      114Marketing / Sociology / Labeling theory / Labelling / Stereotypes / IB / Brand / Professional studies / Communication design

      EGA contribution to the CMDh meeting with interested parties London, 19 May 2015 Variations

      Add to Reading List

      Source URL: www.hma.eu

      Language: English - Date: 2015-05-29 10:18:54
      115Software engineering / Configuration management / Merge / Version control / Marketing authorization / Audio power

      EGA Proposal for Pilot Project on Merging DCPs SUBJECT: CONCEPT of the Pilot Project on Merging DCPs to be proposed to the CMDh for discussion in November 2015 DATE: October 2015

      Add to Reading List

      Source URL: www.hma.eu

      Language: English - Date: 2015-11-27 10:53:14
      116Medicine / Pharmaceutical industry / Summary of Product Characteristics / Clinical pharmacology / Adverse effect / PIL / Health

      CMDh-IP Meeting | London| 19 MayVariation classification of regular updates of SmPC and PIL as regards adverse effects Regular updates of SmPC and PIL – adverse effects

      Add to Reading List

      Source URL: www.hma.eu

      Language: English - Date: 2015-05-29 10:18:52
      117Medical Products Agency / Pharmaceutical industry

      HMA/EMA Task Force on adherence to time tables Christer Backman, MPA 82th HMA MEETING Luxembourg Presidency of the Council of the EU 2015 Dubrovnik, 22-23 October 2015

      Add to Reading List

      Source URL: www.hma.eu

      Language: English - Date: 2015-11-27 10:53:15
      118Clinical data management / Clinical research / Pharmaceutical industry / Quality / Validation / Validity

      EGA contribution to the CMDh meeting with interested parties on DCP improvement London, 18 May 2015 EGA ANNUAL SURVEY ON THE DCP

      Add to Reading List

      Source URL: www.hma.eu

      Language: English - Date: 2015-05-29 10:17:04
      119Software / Pharmaceutical industry / Pharmaceuticals policy / System software / Computer architecture / Drug Master File / Food safety / Qualified person / QP / Good manufacturing practice

      CMDh_340_2015_Rev0_2015 10

      Add to Reading List

      Source URL: www.hma.eu

      Language: English - Date: 2016-01-07 05:29:42
      120Pharmaceutical industry / Medical research / Marketing authorization / Business / Economy / Validation / Email address / Subroutine / Drug Master File

      DOC Document

      Add to Reading List

      Source URL: www.hma.eu

      Language: English - Date: 2015-06-15 05:38:43
      UPDATE