Bioequivalence and Bioavailability Forum

Evidences for GCP Jasim Uddin 2012-08-23 20:52
- Evidences for GCP Debbie 2012-08-24 16:53
- Evidence? Helmut 2012-08-24 19:28
  - Evidence? Jasim Uddin 2012-09-04 12:06

IEC auditing vivekanand 2012-08-27 10:05
- IEC auditing ElMaestro 2012-08-27 10:20

Deviation in Dosing as per Randomisation schedule Mrugank 2012-08-18 18:22
- Double blind – or not? Helmut 2012-08-19 23:47
  - Double blind – or not? Mrugank 2012-08-20 16:37
    - Major protocol deviation Helmut 2012-08-20 16:52

volunteers lab data validity period kaushik089 2012-06-15 08:17
- As short as possible Helmut 2012-06-16 15:46
  - As short as possible kaushik089 2012-06-18 06:00
    - As short as possible drgunasakaran1 2012-06-18 06:49
    - As short as possible Ohlbe 2012-06-18 11:49
      - As short as possible kaushik089 2012-06-19 06:23
        
        As short as possible Helmut 2012-06-19 15:25
        
        As short as possible kaushik089 2012-06-20 05:39
        
        As short as possible Helmut 2012-06-20 14:11

Inclusion and Exclusion criteria Varsha 2012-06-15 12:21
- Inclusion and Exclusion criteria kaushik089 2012-06-15 13:31
  - Inclusion and Exclusion criteria Varsha 2012-06-16 08:40

Criteria check assessment of subjects kapil pandya 2010-11-12 12:43
- Criteria check assessment of subjects Jaime_R 2010-11-12 13:45
  - Criteria check assessment of subjects kapil pandya 2010-11-15 04:49
    - Criteria check assessment of subjects Jaime_R 2010-11-15 14:48
      - Criteria check assessment of subjects Dr_Dan 2010-11-16 11:19
        
        Criteria check assessment of subjects maulik963 2012-05-12 18:11
        
        Criteria check assessment of subjects Dr_Dan 2012-05-14 15:35

Data reviewing process practical 2012-02-17 03:20
- Data reviewing process Ohlbe 2012-02-17 09:55

checking of documents Varsha 2011-05-30 13:45
- checking of documents drgunasakaran1 2011-05-30 21:07
  - checking of documents Varsha 2011-05-31 16:28
- checking of documents Ohlbe 2011-05-30 23:49
  - checking of documents Helmut 2011-05-30 23:57
    - checking of documents Varsha 2011-05-31 16:32
  - checking of documents Varsha 2011-05-31 16:31

QA statement signature jlanteigne 2011-03-02 16:24
- QA statement signature Ohlbe 2011-03-02 17:00
  - QA statement signature jlanteigne 2011-03-02 17:45
    - QA statement signature Helmut 2011-03-02 17:58

C of A M.Vasu 2011-02-10 14:14
- C of A Ohlbe 2011-02-10 16:01
  - C of A M.Vasu 2011-02-10 16:18
    - C of A Ohlbe 2011-02-10 22:31
      - C of A Dr_Dan 2011-02-16 11:00
        
        C of A M.Vasu 2011-02-17 04:24
        
        C of A Dr_Dan 2011-02-17 10:26
        
        C of A Ohlbe 2011-02-21 19:09
        
        C of A Dr_Dan 2011-02-22 09:42

Retention of Sample-USFDA Rajdeep 2010-10-19 12:25
- Retention of Sample-USFDA kapil pandya 2010-11-12 12:38
- Retention of Sample-USFDA Dr_Dan 2010-11-16 11:35

Involvement of ISO auditor 2010-10-28 08:44
- Involvement of ISO ElMaestro 2010-10-28 09:32

Who needs to sign the Protocol raghavendra_s 2010-09-28 13:41

Contracted Phase 1 Trial QA & Compliance raghavendra_s 2010-04-29 11:29
- Contracted Phase 1 Trial QA & Compliance Dr_Dan 2010-04-29 12:14
- Contracted Phase 1 Trial QA & Compliance Ohlbe 2010-04-29 12:14
- Contracted Phase 1 Trial QA & Compliance raghu 2010-04-29 18:23
  - Contracted Phase 1 Trial QA & Compliance Debbie 2010-05-30 18:37
    - Contracted Phase 1 Trial QA & Compliance Dr_Dan 2010-06-02 11:33

master study schedule AKV 2010-05-26 12:14
- Master schedule Ohlbe 2010-05-26 13:54

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