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2018 Data Integrity Seminar : FDA/EU Requirements and Implementation

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Deadline: October 09, 2018 | Date: October 11, 2018-October 12, 2018

Venue/Country: Boston,MA, U.S.A

Updated: 2018-05-04 14:20:31 (GMT+9)

Call For Papers - CFP

2018 Data Integrity Seminar : FDA/EU Requirements and Implementation

Time: 8:30 AM – 4:30 PM


Data Integrity audits project a moving goal post. Issues that were top warning letter vote getters have made way for newer ones to include Cybersecurity etc. Our Data Integrity courses which are offered around the world are renowned for addressing such evolving trends. Consequently, they have attracted record attendances. Attendee feedback suggests the uniqueness of our offerings. Particularly significant is the feedback from those who attended similar courses offered by other companies.

Chinmoy Roy, our course instructor, is one of the world’s first to design, implement and obtain “fit for use” certification for the world’s largest paperless biologics manufacturing facility in the late 1990s. He is a practicing Data Integrity auditor. Former FDA inspectors include him on their 3rd party and mock audit teams. His also continues to provide consulting services in the design and implementation of Data Integrity infrastructures to major multinational companies.

Areas Covered

• What is Data integrity

• Data Life Cycle design and controls

• Elements of a Data Integrity Assurance program

• Roles and responsibilities of different groups in ensuring data integrity

• What data integrity SOPs do auditors expect to see during audits

• Validating Data Integrity

Who will Benefit

• Pharmaceutical industry / Medical device industry / Healthcare industry personnel

• Developers of software for use in Life Sciences industry

• Validation service providers, IT service providers

• Manufacturing personnel, Manufacturing Automation system vendors and system integrators

• Regulatory Affairs group, Quality Unit

• Laboratory personnel

• Users of Cloud

• Clinical Trial Sponsors

Learning Objectives

• Some advanced Data Integrity topics include:

• Data Integrity triad

• Data Integrity Maturity Model

• Developing critical thinking skills

• Data Integrity Audit trends

Speaker Profile

Chinmoy Roy has 37+ years of experience. He is an internationally recognized subject matter expert in CSV, CFR 21 Part 11, Annex 11, Data Integrity and manufacturing process automation systems. He has been invited to speak and conduct training workshops at several international conferences such as ISPE, WBF, Shimadzu’s annual conference for Asia Pacific, etc.

His expertise stems from his experience in implementing and obtaining “fit for use” certification for over 200 IT systems. He has worked at and consulted with leading US based companies such as Roche, Genentech, Bayer, Novartis, Johnson and Johnson etc. His pioneering efforts in implementing CFR 21 Part 11 compliant manufacturing IT systems in 1999 while employed by Genentech, was a precursor to FDA’s issuance of Part 11’s Scope and Application guidance in 2003.

Price: Seminar One Registration $ 1295| Special Group Discount Register for Four attendees $ 3995

Address: Hilton Garden Inn Boston Logan Airport

100 Boardman Street, Boston, Massachusetts 02128 -USA

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.