A JULY SEMINAR OF GMP COMPLIANCE: “REINFORCEMENT AND VISIONS”
The Covid-19 pandemic has passed, leaving a lot of damage behind that affects many aspects of the society in general and the pharma industry in particular. To recover production and business activities, pharmaceutical manufacturers have still made efforts to overcome difficulties, gradually resume production and business activities that were affected to all extents caused by the stagnation due to the pandemic.
However, in pharmaceutical quality management, under any circumstances, GMP compliance and improvement activities aim to improve product quality, help restore production, ensure supply stability, thereby achieving better business results, always placed as a top priority by Top leaders and main staff of most enterprises.
Therefore, for a better understanding of technical matters directly related to the pharmaceutical quality assurance activities that pharma staff may face daily at their production site, with knowledge and experience of GMP compliance from basic to advanced levels, CM Plus Group, with the role of Global GMP Consultant and Pharmaceutical Facility Construction Engineering Designer, once again invite leading experts from Vietnam countrywide and the world back to Ho Chi Minh City to meet up with you and discuss related topics at the annual event of GMP Seminar 2023 on the main subject “GMP compliance in the Post-Covid-19 period: Reinforcement and Visions”. The event will be held on 25th and 26th July 2023 at Caravelle Saigon Hotel, District 1, Ho Chi Minh City.
In the context that a huge number of Vietnamese pharmaceutical companies is looking forward to registration with Stringent Regulation Agencies (SRA) such as EMA, US FDA, etc., good documentation including data Integrity approach to apply for EU-GMP, cGMP, PIC/S GMP certificates is a key concern of manufacturers.
The Seminar is also an opportunity for leading experts in the pharmaceutical industry in Vietnam to share and/or give latest updates of common troubles and errors in data integrity to prove its truthfulness of document contents in drug registration and/or GMP certificate application dossiers.
Welcome all Delegates to the Seminar!
