FDAnews Announces — The 24 Elements You Need For a World-Class Quality…



The 24 Elements You Need For a World-Class Quality Agreement

Jan. 27, 2016 — 1:30 p.m. – 3:00 p.m. EST


Supplier peculiarity is a elemental subject of long-lived importance. Agreements with suppliers strait be created and executed to cover each probable strait and safeguard that a materials that go into a products are accurately what is compulsory and are accessible when needed. Today’s teenager mistake by a retailer could simply spin into tomorrow’s vital recall. And if manuacturers don’t locate all a oversights in a peculiarity agreement, contingency are a FDA will.

On Jan. 27 join Steven Sharf, a 20-year attention maestro who has managed thousands of suppliers for companies like Merck and Novartis, as he explains a 24 elements that strait be enclosed in a peculiarity agreement.

Attendees will not usually learn what a 24 elements are though they will also learn:

  •     The significance of clearly tangible roles in a censure doing / inauspicious eventuality stating process
  •     The need for a shortcoming pattern to clearly brand what entity is obliged for what peculiarity function
  •     How many samples should a agreement need to be retained?
  •     Subcontracting and either a association should concede it during a option of a subcontractor

Don’t consider that since there is no pithy (FDA) requirement for auditing suppliers that manufacturers won’t get created adult in a heartbeat for not carrying a strong review module and peculiarity audits of suppliers.

Meet a Presenter:

Steven Sharf, ASQ-CQA, CPGP

Senior Consultant, Validant

Steven Sharf has spent over 20 years in a curative attention operative on retailer peculiarity government for such companies as Novartis, Merck, and Schering-Plough. Prior to entrance on as Senior Quality Consultant for Validant, he was boss of GMP Concepts and GMP Technical Director for SQA Services. He has managed mixed regions concurrently covering thousands of suppliers and over a hundred auditors, and has worked on mixed agree decrees as an assessor/inspector and a verifier. He has presented on countless occasions to opposite attention groups per a beliefs and philosophies he employs when evaluating suppliers and review programs in general.

Who Will Benefit:

  •     Auditors
  •     Compliance officers
  •     Engineering and pattern controls teams
  •     Executive government
  •     Managers
  •     Manufacturing directors and supervisors
  •     Pharmaceutical and cGMP auditors
  •     QA/QC personnel
  •     Risk government specialists
  •     Strategic formulation and business growth staff
  •     Validation specialists, scientists, engineers

Webinar Details:

The 24 Elements You Need For a World-Class Quality Agreement

Jan. 27, 2016 — 1:30 p.m. – 3:00 p.m. EST



$287 per site

Easy Ways to Register:

Online:     http://www.fdanews.com/24elements

By phone: 888-838-5578 or 703-538-7600

About FDAnews:

FDAnews is a premier provider of domestic and general regulatory, legislative, and business news and information for executives in industries regulated by a US FDA and a European Medicines Agency. Pharmaceutical and medical device professionals rest on FDAnews’ imitation and electronic newsletters, books and conferences to stay in correspondence with general standards and a FDA’s formidable and ever-changing regulations.

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