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SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations

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Website http://bit.ly/2qZ0ecz | Edit Freely

Category FDA Compliance;

Deadline: June 15, 2017 | Date: June 15, 2017-June 16, 2017

Venue/Country: Boston, U.S.A

Updated: 2017-05-10 21:10:57 (GMT+9)

Call For Papers - CFP

One of the best ways to ensure that an organization meets its regulatory obligations is to follow SOPs. SOPs are standardized procedures and processes prepared with enough detail to ensure that tasks are performed consistently each time they are done. SOPs are also required to be in compliance with regulations and guidelines internationally, across all regulated functions. Lack of SOPs and not following SOPs are often cited in regulatory inspections as deficiencies that must be corrected. Poorly prepared SOPs or poor compliance with existing SOPs can compromise a drug development program, an effective quality system, and may result in product recalls.

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Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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