Title 21 CFR Pocket Guides
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Title 21 CFR Part 11 - Available
Newly updated 2008 edition of 21 CFR Part 11 pocket guide - Electronic Records; Electronic Signatures.

List Price$10.00
Member Price$8.00
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Title 21 CFR 58 - Available
Newly updated 2008 edition of Title 21 CFR Part 58 pocket guide - Good Laboratory Practice for Nonclinical Laboratory Studies.

List Price$10.00
Member Price$8.00
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Title 21 CFR Parts 50, 54 & 56 - Available
Newly updated 2008 edition of Title 21 CFR Parts 50, 54 & 56 pocket guide - Protection of Human Subjects, Financial Disclosure by Clinical Investigators and Institutional Review Boards.

List Price$10.00
Member Price$8.00
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Title 21 CFR Parts 201, 202, 203 and 205 - Available
Newly updated 2008 edition of Title 21 CFR Parts 201, 202, 203 & 205 pocket guide – Labeling , Prescription Drug Advertising, Prescription Drug Marketing and Guidelines for State Licensing of Wholesale Prescription Drug Distributers

List Price$10.00
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Title 21 CFR Parts 210 & 211 - Available
Newly updated 2008 edition of Title 21 CFR Parts 210 & 211 pocket guide - Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General; Current Good Manufacturing Practice for Finished Pharmaceuticals.

List Price$10.00
Member Price$8.00
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Title 21 CFR Part 312 - Available
Newly updated 2008 edition of Title 21 CFR Part 312 pocket guide – Investigational New Drug Application.

List Price$10.00
Member Price$8.00
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Title 21 CFR Part 314 - Available
Newly updated 2008 edition of Title 21 CFR Part 314 pocket guide – Applications for FDA Approval to Market a New Drug.

List Price$10.00
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Title 21 CFR Part 316 - Available
Newly updated 2008 edition of 21 CFR Part 316 pocket guide - Orphan Drugs.

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Title 21 CFR Parts 600, 601 & 610 - Available
Newly updated 2008 edition of Title 21 CFR Parts 600, 601 & 610 pocket guide – Biological Products: General; Licensing; General Biological Products Standards.

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Title 21 CFR Parts 606 and 630 - Available
Newly updated 2008 edition of 21 CFR Parts 606 & 630 pocket guide - Current Good Manufacturing Practice for Blood and Blood Components and General Requirements for Blood, Blood Components and Blood Derivatives

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