259 related articles for article (PubMed ID: 17953229)
1. Guidance for temperature-controlled medicinal products: maintaining the quality of temperature-sensitive medicinal products through the transportation environment.
Parenteral Drug Association
PDA J Pharm Sci Technol; 2007; 61(2 Suppl TR 39):2-19. PubMed ID: 17953229
[No Abstract] [Full Text] [Related]
2. Technical report # 39: cold chain guidance for medicinal products: maintaining the quality of temperature-sensitive medicinal products through the transportation environment. Parenteral Drug Association.
PDA J Pharm Sci Technol; 2005; 59(3 Suppl TR39):1-12. PubMed ID: 16313059
[No Abstract] [Full Text] [Related]
3. Integration of temperature-controlled requirements into pharmacy practice.
Ziance R; Chandler C; Bishara RH
J Am Pharm Assoc (2003); 2009; 49(3):e61-7; quiz e68-9. PubMed ID: 19443313
[TBL] [Abstract][Full Text] [Related]
4. WHO Expert Committee on Specifications for Pharmaceutical Preparations. Forty-ninth report.
World Health Organization
World Health Organ Tech Rep Ser; 2015; (992):1-210, back cover. PubMed ID: 26118121
[TBL] [Abstract][Full Text] [Related]
5. WHO Expert Committee on Specifications for Pharmaceutical Preparations.
World Health Organization
World Health Organ Tech Rep Ser; 2014; (986):1-387, back cover. PubMed ID: 24964711
[TBL] [Abstract][Full Text] [Related]
6. Is Lyophilization Key for Transportation and Storage of Biopharmaceutical Drug Products in Space?
Menzen T
J Pharm Sci; 2024 Jul; 113(7):1695-1700. PubMed ID: 38701895
[TBL] [Abstract][Full Text] [Related]
7. Trends in stability testing, with emphasis on stability during distribution and storage.
Kommanaboyina B; Rhodes CT
Drug Dev Ind Pharm; 1999 Jul; 25(7):857-68. PubMed ID: 10459490
[TBL] [Abstract][Full Text] [Related]
8. Stability studies needed to define the handling and transport conditions of sensitive pharmaceutical or biotechnological products.
Ammann C
AAPS PharmSciTech; 2011 Dec; 12(4):1264-75. PubMed ID: 21948319
[TBL] [Abstract][Full Text] [Related]
9. WHO Expert Committee on Specifications for Pharmaceutical Preparations.
World Health Organization Expert Committee on Specifications for Pharmaceutical Preparations
World Health Organ Tech Rep Ser; 2003; 908():i-viii, 1-136, back cover. PubMed ID: 12768889
[TBL] [Abstract][Full Text] [Related]
10. Current good manufacturing practice regulations.
Bumiller J
Bull Parenter Drug Assoc; 1971; 25(5):222-5. PubMed ID: 5094094
[No Abstract] [Full Text] [Related]
11. Certification Scheme on the Quality of Pharmaceutical Products moving in International Commerce.
WHO Chron; 1977 Dec; 31(12):suppl 1-19. PubMed ID: 602166
[No Abstract] [Full Text] [Related]
12. Human and veterinary drugs: good manufacturing practices and proposed exemptions for certain OTC products.
Fed Regist; 1978 Sep; 43(190 Pt 2):45013-89. PubMed ID: 10316700
[No Abstract] [Full Text] [Related]
13. White paper on continuous bioprocessing. May 20-21, 2014 Continuous Manufacturing Symposium.
Konstantinov KB; Cooney CL
J Pharm Sci; 2015 Mar; 104(3):813-20. PubMed ID: 25417595
[TBL] [Abstract][Full Text] [Related]
14. A proposed European pharmacopeia monograph for continuous cell lines derived drugs.
Dorpema JW
Dev Biol Stand; 1989; 70():113-24. PubMed ID: 2759345
[No Abstract] [Full Text] [Related]
15. Container-content compatibility studies: a pharmaceutical team's integrated approach.
Laschi A; Sehnal N; Alarcon A; Barcelo B; Caire-Maurisier F; Delaire M; Feuilloley M; Genot S; Lacaze C; Pisarik L; Smati C
PDA J Pharm Sci Technol; 2009; 63(4):285-93. PubMed ID: 20088243
[TBL] [Abstract][Full Text] [Related]
16. Drug safety: the viewpoint of the pharmaceutical manufacturing industry.
Wigle WW
Can Med Assoc J; 1968 Feb; 98(6):314-7. PubMed ID: 5636099
[No Abstract] [Full Text] [Related]
17. Quality of cold storage drugs transportation and delivery to Thai hospitals.
Sooksriwong CO; Bussaparoek W
J Med Assoc Thai; 2009 Dec; 92(12):1681-5. PubMed ID: 20043573
[TBL] [Abstract][Full Text] [Related]
18. Equipment and analytical companies meeting continuous challenges. May 20-21, 2014 Continuous Manufacturing Symposium.
Page T; Dubina H; Fillipi G; Guidat R; Patnaik S; Poechlauer P; Shering P; Guinn M; Mcdonnell P; Johnston C
J Pharm Sci; 2015 Mar; 104(3):821-31. PubMed ID: 25448273
[TBL] [Abstract][Full Text] [Related]
19. On developing a process for conducting extractable-leachable assessment of components used for storage of biopharmaceuticals.
Wakankar AA; Wang YJ; Canova-Davis E; Ma S; Schmalzing D; Grieco J; Milby T; Reynolds T; Mazzarella K; Hoff E; Gomez S; Martin-Moe S
J Pharm Sci; 2010 May; 99(5):2209-18. PubMed ID: 20039383
[TBL] [Abstract][Full Text] [Related]
20. Pilot study on potential degradation of drug efficacy resulting from Antarctic storage, transport and field conditions.
Priston MJ; Grant IC; Hughes JM; Marquis PT
Int J Circumpolar Health; 2005 Apr; 64(2):184-6. PubMed ID: 15945288
[No Abstract] [Full Text] [Related]
[Next] [New Search]