2005
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Pharmaceutical Sci-Tech


02 January, 2006
11:18 Seasons Greetings A. D'Emanuele
14:59 Growth Promotion Gil Zomber
15:51 RE: Growth Promotion Tony Cundell

03 January, 2006
07:52 Monitoring storage condition for retention sample (AMC vs RH) Yulianda Farraw
16:21 Re: ISO vs GMP javadsha varaiya - rsc
19:47 Assistance with obtaining journal articles that appeared over 10 years ago Michael Anisfeld

04 January, 2006
09:16 Anaerobic monitoring Lritchey
09:17 Tableting Specification Manual vincent.surjana
11:07 RE: ISO vs GMP PB Consultancy
12:47 GMP and cliinical trial material Mark Celeste
18:14 Anaerobic growth testing carol_lampe
21:38 RE: Anaerobic growth testing Jennifer Muncy

05 January, 2006
15:49 Re: GMP and cliinical trial material NORMAN RABIN
15:59 ISO 17025 Atryzek, Vladimir
19:46 Re: ISO 17025 Paul G. King
20:23 RE: ISO 17025 Bob Friedel
21:18 RE: ISO 17025 Atryzek, Vladimir
21:39 RE: Growth Promotion Scott Sutton
23:00 RE: ISO 17025 Bob Friedel
23:08 Sampling raw materials Andy Minkevich

06 January, 2006
08:08 RE: Sampling raw materials Tony Cundell
08:09 Re: Politicized GMPs? Joseph T. Piechocki
09:11 Re: Sampling raw materials Paul G. King
16:30 URS Brooks
16:31 Polysorbate 80 sampling and testing Andy Minkevich
16:41 Growth Promotion Andy Minkevich
17:48 RE: URS Les Edwards
17:48 Re: URS Jeremy.Court

07 January, 2006
00:40 Re: Sampling raw materials Stanley110

08 January, 2006
11:14 Deadly Medicine? Michael Brown
11:15 Re: Politicized GMPs? Michael Brown
15:56 Re: URS Mark Celeste

10 January, 2006
11:57 Product Bubble point in integrity testing Saritha Devi Polturi
13:08 Re: Product Bubble point in integrity testing h.van doorne
14:07 Re: Product Bubble point in integrity testing etiennet
14:09 Re: Product Bubble point in integrity testing Jim Tyrrell
16:29 RE: Product Bubble point in integrity testing Alan.Moon

11 January, 2006
15:17 When should we passivate to remove rouge? Robert Loss
17:28 RE: When should we passivate to remove rouge? McConlogue, Liam

12 January, 2006
09:22 Moisture Issue with Vacuum Dried Product finbar oneill
10:38 RE: Moisture Issue with Vacuum Dried Product Søren Bogø
10:39 RE: Moisture Issue with Vacuum Dried Product Tully, Roger
10:40 RE: Moisture Issue with Vacuum Dried Product skachhwaha
11:09 Decimals number of impurity in API Hiroaki Matsumoto
11:26 RE: When should we passivate to remove rouge? Thomas Peither
12:11 Re: Decimals number of impurity in API Brian MATTHEWS
15:32 RE: Moisture Issue with Vacuum Dried Product Barry Giordano
15:32 Ampoules integrity testing method Papailiou Nikos
15:33 Re: Decimals number of impurity in API Jim Tyrrell
16:22 RE: GMP and cliinical trial material Post, Ivar
18:25 RE: When should we passivate to remove rouge? Daryl Roll
18:25 RE: When should we passivate to remove rouge? Daryl Roll
22:20 Re: When should we passivate to remove rouge? GCampbell

13 January, 2006
04:05 Re: Decimal number of Impurity in API r.kirsch
07:36 Re: Decimals number of impurity in API ravindra goyal
07:37 Re: Ampoules integrity testing method etiennet
13:26 Re: Ampoules integrity testing method JFolan
16:07 R: Ampoules integrity testing method Mari, Alberto

15 January, 2006
09:31 Re: Decimals number of impurity in API himanshu
14:30 Re: GMPs and Clinical Trial Material william scruggs

16 January, 2006
06:21 RE: GMPs and Clinical Trial Material Michael Anisfeld
13:22 RE: GMPs and Clinical Trial Material Mark Celeste
14:41 RE: GMPs and Clinical Trial Material David Perkins
14:50 RE: GMPs and Clinical Trial Material Miguel Castellanos
14:51 Antisera and clinical trials Gil Zomber
15:18 RE: GMPs and Clinical Trial Material Nancy Fulginiti
15:19 Re: GMPs and CTM William Scruggs
17:50 RE: GMPs and Clinical Trial Material Andrew Minkevich
20:53 RE: GMPs and Clinical Trial Material Frank Rauschen

17 January, 2006
07:53 SIP requirements for temperature Chip Schenk
11:16 RE: Moisture Issue with Vacuum Dried Product finbar oneill
15:31 RE: SIP requirements for temperature McConlogue, Liam
21:06 Re: SIP requirements for temperature Jim Tyrrell
21:56 RE: Growth Promotion Scott Sutton

18 January, 2006
21:18 Expectations of Sanitation Effectiveness Robert Rosenlof

19 January, 2006
19:45 FDA 2656 Rajagopal

20 January, 2006
08:15 Visual Inspection of uncoated tablets ravindra goyal
18:20 Cleaning Reagents Tom Smith
18:20 WFI Loop Temp bens
18:20 Environmental Monitoring for Clinical APIs Cheryl Loomis
18:20 Raw material specifications and process validation Jean-Philippe Cros
19:02 Re: Environmental Monitoring for Clinical APIs NORMAN RABIN
19:03 Re: WFI Loop Temp NORMAN RABIN
19:37 Non-Sterile APIs Miguel Castellanos
19:38 Re: Cleaning Reagents Bob Kirsch
20:02 Re: Raw material specifications and process validation Paul G. King
20:03 RE: WFI Loop Temp Kenyon, David [CNTUS]
20:11 Anti-static devices Connie Hillenbrand
20:59 Schott vials Ron Herman
21:00 Re: Anti-static devices Bob Kirsch

21 January, 2006
08:37 Re: Raw material specifications and process validation Dr Moustsfa Al Shammat
08:39 Parameters for delaying the filtration process for Injectables Saritha
08:57 RE: WFI Loop Temp Pradeep Chakravarty - Claris
11:45 RE: Parameters for delaying the filtration process for Injectables ratnakar.salunke
15:11 Instruments Qualification Mohammad Musbah
15:31 RE: Non-Sterile APIs Michael Anisfeld
15:50 RE: Parameters for delaying the filtration process for Injectables Jornitz, Maik
18:58 Re: Instruments Qualification Bob Kirsch
23:06 Re: Anti-static devices Stanley110

23 January, 2006
10:58 Required microbial and BET limits for API P.Saritha Devi

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