One of the highest standards of laboratory equipment is 21 CFR Part 11.FDA issued 21 CFR Part 11 regulations in 1997, outlined criteria for acceptance of electronic records, electronic signatures, and handwritten signatures. The regulation allows electronic records to be considered equivalent to paper records and handwritten signatures.However, there are not plentiful 21 CFR Part 11 qualified devices for one simple reason: They still have BUTTONS and SWITCHES! Their manufacturers are blocking themselves from innovation and satisfying & meeting new customers.But has your laboratory equipment fulfilled the 21 CFR Part 11?Do you want to exceed the expectations and deliver an excellent piece of laboratory equipment for your customers? We - Certos - are happy to be a partner to assist you.Visit us: www.certos.aiContact us: support@certos.ai

The Pharma professionals and associations across Latin America are gathering at the Pharma Corporate Compliance Latam 2018 Congress to know the latest updates on compliance by top experts and executives.

The event will take place at the Tivoli Mofarrej São Paulo Hotel, Brazil on June 13th and 14th.

• Topics: Regulations, Case Studies, GxP, Third party interactions. Get the free PDF Agenda https://goo.gl/mC89Xw

• With the support of Anvisa and the Ministry of Transparency, Supervision and Control Comptroller General (CGU), Brazil.

• The Congress is suitable for professionals in the areas of: Compliance, Legal, Regulatory, Public Affair, Quality and Management.

Watch Video: https://goo.gl/YmypGU

Go to Website: https://goo.gl/GUQXDd

Register Online: https://goo.gl/yyL4RR

At the end of 2017, the MHRA published its latest GDP deficiency data and listed quality systems and transportation as the top categories for major deficiencies. Although medical authorities continue to push the advancement of supply chain quality and security, it is still a minefield to navigate.

We created the Pharma Logistics Compliance 2018 Report designed specifically to keep you up to date with key developments that we believe will shape the compliance agenda over the next year.

View the report>> http://bit.ly/2K4oALz

Don’t miss out on special features including:
-Supply Chain Security and Traceability – GPS
-Brexit
-ICH Q12 Flexibility Initiatives
-EMA Regulations
-Emerging Markets and Regulations
-And more

View the report >> http://bit.ly/2K4oALz

Interested in learning more about compliance? This topic will be covered in case studies and session at the 16th Annual Cold Chain Global Forum this September 24-27.

Find out more >> http://bit.ly/2jD7rNQ

Join us and top pharma supply chain executives to address end-to-end supply chain optimization and create strategies to remain complaint with regulatory agencies, ensure quality compliance, and implement customer centricity to enhance patient first initiatives.

Hope to see you there!

The Cold Chain Global Forum Team
September 24-27, 2018
Philadelphia Convention Center, Philadelphia