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Pharmaceutical Manufacturing Equipment Qualification And Maintenance

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Deadline: April 22, 2020 | Date: April 22, 2020

Venue/Country: U.S.A

Updated: 2019-11-07 23:22:52 (GMT+9)

Call For Papers - CFP

Attend this webinar to learn about the GMP requirements for pharmaceutical equipment. Regulations require that equipment is to be of appropriate design, constructed not to alter the product, and properly cleaned and maintained. Demonstrating the adequacy of the equipment starts with a risk assessment and a design qualification and continues through installation qualification, operational qualification, performance qualification and process validation. Preventive and corrective maintenance provide assurance that the equipment will continue to operate as intended.

Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.