The Global Pharma Regulatory Affairs Online Certification Course gives a wonderful opportunity to the student to learn something amazing and new about the manufacturing of a drug till its registration across the Globe.

The Global Pharmaceutical Regulatory Affairs Professional Certification Programme promises to provide amazing foundation-level and higher level training from FRESHER till INDUSTRY WORKING PROFESSIONALS.

It is a perfect introduction for entrants fresh to the sector of pharmaceutical regulatory affairs. It speaks about the main needs required to keep and gain approval to post approval medicinal products in Europe and the USA and other ROW countries!

The prime role of major players as well as the legal framework are shown under Global RA course!

The programme covers the journey of the manufacturing process of a drug. The multiple procedures offered for approval and assessment of products are shown, and their special needs are covered and described. Important terms that are required to be filled out for the post-marketing endorsement are also outlined.

With the change in the process as well as the regulations taken place, the plan is rightly updated and serves as a wonderful reference tool that lets not just the new users but even professional users keep them updated with the broader image of the environment of regulatory affairs.

This special programme of GRA comprises information about the API, Formulation, Medical Devices, Biotech products, OTC, etc.

For example, EU procedures comprises of

• De-centralized process (DCP),
• EU variation process,
• The mutual recognition process (MRP),
• The European centralized process (CP);
• Requirements for obtaining approval for a new drug in the USA (the NDA process)
• For grabbing approval from the FDA for generic items in the USA (the ANDA),
• Electronic technological paper (CTD);
• Doing the right submissions in the ordinary technical document (CTD);
• Orphan drug requests in the US and EU;
• Important for human medicinal items in the US and EU;
• Registration of monoclonal antibodies.

If you are willing to take admission in the programme, you will be enrolled in the below-mentioned regulatory affairs courses. Like

• RA-API,
• RA-Formulation
• Global RA
• CTD/eCTD/ ACTD submissions

Completing them is mandatory to complete the RA programme.

• Explore the dynamic world of regulatory affairs API (Drug Substances) and its significance in the pharmaceutical landscape.
• Characterization and polymerization of API: Delve into the crucial processes that define the quality of active pharmaceutical ingredients.
• Drug Substance Regulation: Uncover the intricacies of DMF, ASMF, and CEP, understanding the backbone of regulatory compliance.
• Regulation in Semi-Regulated Countries: Navigate the complexities of regulatory frameworks in emerging markets.
• DMF Submission in CTD/ACTD Format: Master the art of preparing and submitting drug master files in globally recognized formats.
• 21 CFR Part 11 and its Importance: Grasp the significance of compliance in electronic records and signatures.
• Regulations in Regulated Markets (USA, EU, etc.): Gain insights into the regulatory landscapes of major markets, ensuring global compliance.
• Regulations in Semi-Regulated Markets (ROW Countries): Understand the unique challenges and opportunities in markets across the globe.
• DMF Submissions in CTD/eCTD/ACTD Formats: Navigate through the technicalities of various submission formats for seamless approvals.
• Life Cycle Management: Explore strategies for effective life cycle management, ensuring ongoing regulatory compliance.

So, if you are interested in the Global Pharma Regulatory Affairs or RA- API, RA- Formulations etc.

We do have all Online Certification Course, ANYTIME from ANYWHERE

It is better to collect more information about the course online at www.raajpharmaelearning.com