Your future depends on using data in ways you’ve never imagined. Join us for a morning of insights, inspiration, value—and breakfast—where you’ll learn all about the Snowflake Data Cloud. During this event you’ll learn: How to unsilo disparate data and enable your most critical data workloads How to connect globally to data and data service providers to extract untold business value How organizations such as yours...

We have all heard of Data Integrity but do you really understand what it is? Do you understand how 21 CFR 11 and Annex 11 fit into this picture? Specifically, can you answer questions on the following? Evolution of 21 CFR Part 11 and Annex 11 and Why they are Back in the News Overview and Key Requirements of Part 11 & Annex 11 How to use a Risk Based Assessment to reduce work while still achieving Data Integrity and Compliance? How FDA ...

Overview: Quality control and related contract laboratories are considered at high risk because after testing and approval, drug products and Active Pharmaceutical Ingredients (APIs) are released to the market without further check. That's the reason why the FDA and other agencies put highest emphasis on inspections of QC laboratories. Even though cGMP regulations have been in place since long time, the large number of QC related 483's and war...

India Security Conference is your networking platform to interact with the security community and learn about the security challenges and latest security innovations and solutions. Themed “Building safe and secured environments with Intelligence, Analytics and Mobility”, the event will focus on cybersecurity and safe cities issues. Co-located with InfoComm India - India’s premier exhibition and conference for the professiona...

Overview: Analytical equipment should be qualified and computer systems should be validated to demonstrate suitability for the intended use. Electronic records must comply with FDA Part 11 and EU/PICS GMP Annex 11 requirements to ensure data integrity, security and availability. Recent EU and FDA inspection documents prove that qualification, validation and electronic laboratory are records are on target of inspectors. The large number of warn...

Argus is delighted to launch the next Argus Asian Petroleum Coke 2015 conference in Mumbai, India. India is seen as the next big petroleum coke importer by 2016. Coal shortages, combined with domestic refiner Reliance Industries (RIL) preparing to start up its gasification project next year, mean RIL and cement companies are now looking to the US for their supply replacements. Join all from the petroleum coke industry and gain in-depth knowled...

A Business to Business event which brings together construction professionals from around the world. A showcase of both international and local construction products are on display.The event offers all visitors and exhibitors free to attend seminar sessions taking place during the 3 days of the show. Exhibitors would meet with Architects, Consultants, Engineers, Builders, Contractors, Developers and Interior Designers.

2013 has been a crucial year for the Indian pharmaceutical industry as most of the top pharmaceutical companies had serious allegations related to 'data-fudging’ reported by FDA's Centre for Drug Evaluation and Research. Major issues noticed by the regulators during inspection include: Established laboratory controls are not followed and data is not recorded at the time of performance Deviations from written test procedures are not recor...

The pharmaceutical industry has encountered major shifts in recent years, both within the industry and in its external environment. Some of the factors responsible for this shift include the rising cost of healthcare due to an aging population, the increase in rigorous regulatory requirements, and company mergers within the industry. These factors have led to an increased need for restructuring, cost reduction and culture change projects. Coor...

Ensuring Failure Free Sterility Assurance and Audits For Your Sterile Product and Facilities Sterile Pharma Workshop Would Answers Your Problems Regarding:• Sterility Assurance• Sterility Validation• Audits in sterile plantsFormat of Sterile Pharma WorkshopWorkshop Day One:• Sterility assurance• Case study discussion• Group exercises• Cross functional situation role playWorkshop Day Two:• Sterility valid...