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The 'An Introduction to Upstream and Downstream Manufacturing in the Biopharmaceutical Industry Training Course' is an online workshop organized by Management Forum Ltd, aimed at providing a comprehensive overview of the biomanufacturing processes within the pharmaceutical industry. This training course is designed to cater to professionals seeking to deepen their
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understanding of how scientific innovations in the biopharmaceutical sector are transformed into therapeutic products. Attendees can expect to gain insights into the entire drug development process, which spans from initial research through to the market launch of new medicines.
Participants will engage in discussions surrounding key topics such as molecule discovery, preclinical testing, clinical trials, and the regulatory frameworks governing the biopharmaceutical industry. The course emphasizes the critical stages of bioprocessing, detailing both upstream and downstream processes. Upstream processing focuses on optimizing conditions for cell cultures and microorganisms to yield target products, while downstream processing is concerned with purification and formulation to ensure product safety and quality. The interconnected nature of these processes means that understanding the complexities involved can significantly enhance operational efficiency and product consistency.
As part of the workshop, attendees will also learn about best practices in maintaining product quality, including process validation, quality assurance, and compliance with regulatory bodies such as the FDA and EMA. Insight into innovative solutions for common industry challenges, as well as the latest technological advancements like automation and artificial intelligence in biomanufacturing, will be explored. This training course is suitable for various professionals, including Quality Assurance and Control (QA/QC) personnel, R&D team members, project managers in biotechnology and pharmaceuticals, supply chain and logistics teams, and senior leadership such as CTOs and VPs of Operations. The course also welcomes students and trainees in biotechnology and pharmaceutical sciences, as well as Environmental Health and Safety (EHS) personnel.
The workshop will feature Mustafa Edik, an Independent GMP Consultant and Auditor with over 25 years of experience in the industry. Edik has a rich background in Quality Assurance and has trained thousands of professionals in GMP, GDP, and Pharmaceutical Quality Management Systems. His expertise and practical insights promise to provide attendees with valuable knowledge and tools to navigate the complexities of upstream and downstream manufacturing processes in the biopharmaceutical field. Participants will have opportunities to interact with Edik and fellow attendees, enhancing the learning experience, and will receive documentation and certification of completion upon finishing the course. This training course offers a unique opportunity to turn a lunch hour into a productive learning experience, combining budget-friendly options with flexible scheduling tailored to busy professionals.
Participants will engage in discussions surrounding key topics such as molecule discovery, preclinical testing, clinical trials, and the regulatory frameworks governing the biopharmaceutical industry. The course emphasizes the critical stages of bioprocessing, detailing both upstream and downstream processes. Upstream processing focuses on optimizing conditions for cell cultures and microorganisms to yield target products, while downstream processing is concerned with purification and formulation to ensure product safety and quality. The interconnected nature of these processes means that understanding the complexities involved can significantly enhance operational efficiency and product consistency.
As part of the workshop, attendees will also learn about best practices in maintaining product quality, including process validation, quality assurance, and compliance with regulatory bodies such as the FDA and EMA. Insight into innovative solutions for common industry challenges, as well as the latest technological advancements like automation and artificial intelligence in biomanufacturing, will be explored. This training course is suitable for various professionals, including Quality Assurance and Control (QA/QC) personnel, R&D team members, project managers in biotechnology and pharmaceuticals, supply chain and logistics teams, and senior leadership such as CTOs and VPs of Operations. The course also welcomes students and trainees in biotechnology and pharmaceutical sciences, as well as Environmental Health and Safety (EHS) personnel.
The workshop will feature Mustafa Edik, an Independent GMP Consultant and Auditor with over 25 years of experience in the industry. Edik has a rich background in Quality Assurance and has trained thousands of professionals in GMP, GDP, and Pharmaceutical Quality Management Systems. His expertise and practical insights promise to provide attendees with valuable knowledge and tools to navigate the complexities of upstream and downstream manufacturing processes in the biopharmaceutical field. Participants will have opportunities to interact with Edik and fellow attendees, enhancing the learning experience, and will receive documentation and certification of completion upon finishing the course. This training course offers a unique opportunity to turn a lunch hour into a productive learning experience, combining budget-friendly options with flexible scheduling tailored to busy professionals.
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Estimated Turnoutupto 100 Delegates Based on previous editions | Official LinksWebsiteContacts
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EditionsSep 2025 Interested+1 more edition Frequency Bi-annual | Report Error Claim this event |
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