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Welcome to the GMP Discussion Forum.

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List of contributions:

sterility testing from Nadia (10/7/2008 08:27)
limits for impurities from Tareq Taha (10/7/2008 00:34)
Import testing from Z Pawlak (10/3/2008 20:05)
- RE: Import testing from JD Mallet (10/4/2008 11:24)
  - RE: RE: Import testing from Z Pawlak (10/7/2008 09:47)
integrity testing from tanja (10/2/2008 16:35)
- RE: integrity testing from Dick Bonner (10/5/2008 13:18)
  - RE: RE: integrity testing from tanja (10/7/2008 11:32)
- RE: integrity testing from ok (10/4/2008 14:45)
Topics covered in GMP Discussion forum from Dr.V.P.Barve (9/30/2008 14:13)
- RE: Topics covered in GMP Discussion forum from JD Mallet (10/4/2008 11:17)
UKMHRA and USFDA from amirhossein (9/29/2008 15:54)
- RE: UKMHRA and USFDA from JD Mallet (9/29/2008 20:25)
INTEGRITY TESTING from Archana Verma (9/28/2008 14:15)
- RE: INTEGRITY TESTING from JD Mallet (9/29/2008 09:24)
  - RE: RE: INTEGRITY TESTING from Archana Verma (10/5/2008 15:41)
Dissolution from DissoTester (9/27/2008 18:37)
- RE: Dissolution from Ian (9/29/2008 19:28)
pH converter from lisa (9/26/2008 10:00)
- RE: pH converter from JD Mallet (9/29/2008 09:35)
bioburden validation from samatha (9/25/2008 13:00)
- RE: bioburden validation from Archana (9/27/2008 17:09)
- RE: bioburden validation from JD Mallet (9/25/2008 13:31)
clean room wash area from Babu (9/23/2008 18:49)
- RE: clean room wash area from JD Mallet (9/24/2008 06:47)
Cytotoxic Drug Substance from KNITI (9/23/2008 06:30)
- RE: Cytotoxic Drug Substance from JD Mallet (9/23/2008 16:57)
  - RE: RE: Cytotoxic Drug Substance from KNITI (9/24/2008 06:29)
    - RE: RE: RE: Cytotoxic Drug Substance from JD Mallet (9/24/2008 06:42)
      - RE: RE: RE: RE: Cytotoxic Drug Substance from KNITI (9/24/2008 09:28)
        RE: RE: RE: RE: RE: Cytotoxic Drug Substance from JD Mallet (9/24/2008 15:00)
        RE: RE: RE: RE: RE: RE: Cytotoxic Drug Substance from NH ESWARA PRASAD (9/29/2008 19:03)
ANTIBIOTIC-MICROBIAL ASSAY from lisa (9/23/2008 06:26)
clean rooms from Babu (9/22/2008 19:03)
- RE: clean rooms from NH ESWARA PRASAD (9/29/2008 19:06)
french introduction about us cgmp? from ok (9/22/2008 11:54)
- RE: french introduction about us cgmp? from ok (9/24/2008 07:17)
  - RE: RE: french introduction about us cgmp? from ok (9/25/2008 07:11)
  - RE: RE: french introduction about us cgmp? from JD Mallet (9/24/2008 15:06)
- RE: french introduction about us cgmp? from JD Mallet (9/22/2008 19:35)
software validation from Tareq Taha (9/20/2008 23:19)
- RE: software validation from JD MALLET (continued) (9/22/2008 18:07)
production activity when no qa or qc personnel on duty from M.BADR (9/19/2008 23:28)
- RE: production activity when no qa or qc personnel on duty from Rui (9/22/2008 08:54)
- RE: production activity when no qa or qc personnel on duty from mradul gupta (9/20/2008 06:35)
usp monograph from Tareq Taha (9/18/2008 00:18)
- RE: usp monograph from Bernd Renger (9/19/2008 09:21)
lamotrigine from Tareq Taha (9/17/2008 22:35)
- RE: lamotrigine from Bernd Renger (9/19/2008 09:26)
periodic passivation of PW loop from Rui (9/17/2008 02:15)
- RE: periodic passivation of PW loop from Federal GMP Regulator (9/18/2008 04:56)
Cell line for manufacturing of DC vaccine from Daniela Rozkova (9/16/2008 15:38)
- RE: Cell line for manufacturing of DC vaccine from Roy Cowell (9/16/2008 20:01)
Temperature mapping from ramesh (9/15/2008 11:49)
- RE: Temperature mapping from Roy Cowell (9/15/2008 17:17)
  - RE: RE: Temperature mapping from Federal GMP Regulator (9/18/2008 04:52)
    - RE: RE: RE: Temperature mapping from Dr.V.P.Barve (9/20/2008 14:35)
related substances from Tareq Taha (9/12/2008 23:19)
- RE: related substances from Dr.V.P.Barve (9/15/2008 07:02)
- RE: related substances from Roy Cowell (9/13/2008 17:18)
  - RE: RE: related substances from Archana Verma (9/27/2008 17:19)
clean rooms from Babu (9/12/2008 18:25)
- Clean Rooms from Federal Regulator (9/18/2008 04:49)
analytical method transferring validation from ok (9/12/2008 07:49)
- RE: analytical method transferring validation from Bernd Renger (9/17/2008 18:36)
new cgmp of us from ok (9/12/2008 07:46)
homogeneity from mohsen (9/11/2008 13:41)
- RE: homogeneity from Roy Cowell (9/11/2008 15:02)
in-process control for coating tablet from Dvid (9/11/2008 03:26)
- RE: in-process control for coating tablet from mradul gupta (9/20/2008 06:39)
- RE: in-process control for coating tablet from Roy Cowell (9/11/2008 13:32)
- RE: in-process control for coating tablet from Bernd Renger (9/11/2008 13:19)
pharmacopeial method from Tareq taha (9/8/2008 23:09)
- RE: pharmacopoeial method from Roy Cowell (9/10/2008 13:40)
- RE: pharmacopeial method from Bernd Renger (9/9/2008 13:43)
  - RE: RE: pharmacopeial method from Tareq Taha (9/9/2008 23:06)
    - RE: RE: RE: pharmacopeial method from JD Mallet (9/10/2008 08:37)
      - RE: RE: RE: RE: pharmacopeial method from Dr.V.P.Barve (9/10/2008 09:27)
        RE: RE: RE: RE: RE: pharmacopeial method from Bernd Renger (9/10/2008 10:27)
Identification of Coloring Agents in Dosage Forms from Dr.V.P.Barve (9/5/2008 08:40)
- RE: Identification of Coloring Agents in Dosage Forms from Tareq Taha (9/12/2008 23:14)
  - RE: RE: Identification of Coloring Agents in Dosage Forms from Dr. V.P.Barve (9/13/2008 08:47)
- RE: Identification of Coloring Agents in Dosage Forms from JD Mallet (9/10/2008 08:41)
  - RE: RE: Identification of Coloring Agents in Dosage Forms from Dr.V.P.Barve (9/10/2008 09:14)
Stability from J. Geeven (9/2/2008 13:32)
- RE: Stability from Sophia (9/3/2008 03:19)
Newly revised Chinese GMP from JD Mallet (8/30/2008 20:14)
- RE: Newly revised Chinese GMP from Fiona (9/1/2008 08:12)
  - RE: RE: Newly revised Chinese GMP from ok (9/5/2008 10:17)
TREND ANALYSIS from gagandeep kaur (8/30/2008 08:05)
- RE: TREND ANALYSIS from N H Eswara Prasad (8/30/2008 10:21)
Stability studies - orientation of samples from shekhar dabholkar (8/29/2008 10:33)
- RE: Stability studies - orientation of samples from T.R.Narayanappa (9/1/2008 08:36)
Method validation from Wamba (8/27/2008 12:31)
- RE: Method validation from Archana Verma (10/5/2008 18:24)
- RE: Method validation from Tareq taha (9/8/2008 22:59)
- RE: Method validation from Bernd Renger (8/27/2008 15:24)
ANY PHARMA COURSE AFTER BSC from SONIA (8/22/2008 12:39)
VAlidation protocol from Sejal (8/22/2008 08:08)
- RE: VAlidation protocol from Canada Man (8/23/2008 00:43)
  - RE: RE: VAlidation protocol from narendra patil (9/14/2008 10:42)
Qualified Person from KNITI (8/22/2008 05:54)
- RE: Qualified Person from Bernd Renger (8/27/2008 15:09)
  - RE: RE: Qualified Person from KNITI (8/28/2008 06:27)
- RE: Qualified Person from JD Mallet (8/22/2008 16:43)
antiretrovirals from s ghosh (8/21/2008 08:39)
- RE: antiretrovirals from JD Mallet (8/22/2008 04:12)
shelf life from gagandeep kaur (8/20/2008 10:38)
- RE: shelf life from Dick Bonner (8/24/2008 20:48)
- RE: shelf life from Dick Bonner (8/20/2008 20:10)
  - RE: RE: shelf life from abuamameed (8/20/2008 22:12)
OOS results from Domenico Demasi (8/19/2008 22:28)
- RE: OOS results from Bernd Renger (8/20/2008 13:20)
  - RE: RE: OOS results from Domenico Demasi (8/20/2008 22:27)
    - RE: RE: RE: OOS results from Bernd Renger (8/26/2008 09:15)
labelling all areas in a pharmaceutical plant from sandra (8/15/2008 14:37)
- RE: labelling all areas in a pharmaceutical plant from JD Mallet (8/22/2008 04:07)
- RE: labelling all areas in a pharmaceutical plant from Michael Cutter (8/18/2008 11:26)
non active rm from gagandeep kaur (8/11/2008 10:40)
- RE: non active rm from Dick Bonner (8/20/2008 20:09)
regulatory GMP inspection history at API suppliers from Neil C (8/7/2008 16:09)
- RE: regulatory GMP inspection history at API suppliers from Jan Schuler (8/20/2008 00:33)
- RE: regulatory GMP inspection history at API suppliers from abuamameed (8/19/2008 22:19)
  - RE: RE: regulatory GMP inspection history at API suppliers from brenger (8/26/2008 09:24)
CEP / Health-Authorities Inspection / Supply API from York Moeller (8/6/2008 04:26)
- RE: CEP / Health-Authorities Inspection / Supply API from Iverson (9/12/2008 07:01)
Stability of opened containers from K. Mackin (8/4/2008 13:02)
- RE: Stability of opened containers from Ian (8/5/2008 13:25)
- RE: Stability of opened containers from Camelia (8/4/2008 14:51)
Purified water from other facility from Rocky Bell (8/4/2008 07:14)
- RE: Purified water from other facility from N.H.Eswara Prasad (8/27/2008 16:10)
- RE: Purified water from other facility from Ian (8/11/2008 19:36)
  - RE: RE: Purified water from other facility from JD Mallet (8/16/2008 08:07)
Sample jar glass grades from M Murphy (8/1/2008 18:28)
- RE: Sample jar glass grades from Camelia (8/4/2008 14:56)
  - RE: RE: Sample jar glass grades from M Murphy (8/5/2008 12:35)
Animal Origin from N H Eswara Prasad (7/31/2008 19:04)
- RE: Animal Origin from Ganesh Nomulwar (8/1/2008 12:42)
usfda guidelines from gagandeep kaur (7/31/2008 10:18)
- RE: usfda guidelines from M Murphy (7/31/2008 12:44)
  - RE: RE: usfda guidelines from Dr N Singh (8/1/2008 10:22)