WORKSHOP ON CSV, DATA INTEGRITY AND 21 CFR PART 11 2017 - Seminar on Computer Systems Validation (CSV), Data Integrity, 21 CFR Part 11 Compliance and GAMP 5
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Website http://compliancetrainings.in/product/computer-systems-validation-csv-data-integrity-21-cfr-part-11- |
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Category pharmaceutical; data integrity; CSV; FDA; 21 CFR; annex 11; glp; validation; Electronic Signatures; Warning Letters; 483s; ALCOA
Deadline: April 15, 2017 | Date: April 18, 2017-April 19, 2017
Venue/Country: Hyderabad, India
Updated: 2017-02-14 00:17:53 (GMT+9)
Call For Papers - CFP
This new 2-day Seminar on Computer Systems Validation provides participants with knowledge and tools to effectively use, monitor, control, and assure the integrity of electronic data and computerized systems. The presenter - Mr. KR Vaghela will help you explore proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments.The course not only ensures a full understanding of the regulations and guidelines for raw data and other records but also provides templates and examples to develop inspection ready documentation. Interactive exercises will be dispersed into and between the presentations.Areas Covered:Role of FDAComputer Systems Validation PointsWhy Validation?Benefits of ValidationGAMP 521 CFR Part 11 ComplianceAnnex 11Data IntegrityRelated Warning Letter PointsComputer Systems Validation DeliverablesRisk Assessment ….and MoreA must attend seminar for professionals in:Pharmaceutical Development CompaniesQuality Control Laboratories CompaniesQuality Departments of API ManufacturersQuality Departments of Finished Product ManufacturersMedical Device CompaniesBiotech CompaniesContract LaboratoriesClinical Research OrganisationsSuppliers and Service Providers of Instruments and Computer SystemsEvery Company that needs to comply with FDA Regulations
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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