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Canada

no at no company from Germany

CEO at Pnj Sharptech Computing Services from India

Hi, I am Ranjan here working as a social media expert. Are you looking for SMO Services at an affordable price? So, your search end we are providing the best SMO services at a reasonable price.

digital marketing at spin on education from India · Greater Noida

Hi, I am Kanak Rathor. I am an educational consultant in an India-based company. If you are looking for all kinds of details about it. After doing the MBA colleges in Lucknow., you must have a look at our website. You will get all the details including exam preparation, syllabus, exam date-sheet, cut-off, and other things in detail. Visit our website for more information.

Innovation Consultant from Australia

Biomaterials Manager at FPInnovations from Canada

CEO at AdvanceEra from United States · calgary

Innovation Manager from United Kingdom

Greetings for the day! This side is Ethan Hernandez. I am a Technical Engineer of Support for emails. I have 2 years of experience in solving problems related to outlook. Are you facing the issue of Outlook attachments not showing in emails? It may be because of some issues going on with your account. Email or Call us for an instant solution.

president & chief consultant at sumimoto packaging consultant office from Japan

Process Validation for Biotechnological Products - EU edition MasterClass

Process Validation for Biotechnological Products - EU edition MasterClass

22 - 23 November, 2022

Online Event

Process Validation for Biotechnological Products MasterClass aims to provide deeper understanding on how process validation for biotechnological processes, which is the collection and evaluation of data from the process design stage through commercial production....

  • +4 months
Pharmaceutical Reference Standards - EU edition MasterClass

Pharmaceutical Reference Standards - EU edition MasterClass

22 - 23 November, 2022

Online Event

Reference standards are an essential tool in the quality control of APIs (active pharmaceutical ingredients), excipients and medicinal products. They may be obtained from official sources or may, under certain circumstances, be developed and maintained in-house. In this training course you will learn about the correct use of official (pharmacopoeial) standards and regulatory requirements but also about the possiblity to establish in-house standar...

  • +4 months
Cross-contamination Risk Assessment in Pharmaceutical Manufacturing - EU edition MasterClass

Cross-contamination Risk Assessment in Pharmaceutical Manufacturing - EU edition MasterClass

21 - 22 November, 2022

Online Event

It is common practice in the Pharmaceutical Industry to manufacture multiple drug products in shared facilities with shared equipment. To avoid cross-contamination, all surfaces with product contact are cleaned prior to manufacturing of the subsequent product. According to current EU GMP requirements, the cleaning process has to be validated taking into account the API specific PDE (“Permitted Daily Exposure”) values. The EMA “Guideline on ...

  • +4 months
GAMP® 5 - US edition MasterClass

GAMP® 5 - US edition MasterClass

21 - 22 November, 2022

Online Event

In this Master Class, we will review the current trends, including in technology and in FDA compliance and enforcement. We’ll look at Data Integrity, 21 CFR Part 11 (Electronic Records/Electronic Signatures), European Union (EU) Annex 11, General Data Protection Regulation (GDPR), and other regulatory requirements....

  • +4 months

Director from United Kingdom

Entry Level CMC - US edition MasterClass

Entry Level CMC - US edition MasterClass

21 - 22 November, 2022

Online Event

Chemistry, Manufacturing and Control (CMC) is key in the development and routine production of a medicinal product, and this course helps you understand the basic requirements and how to reflect them in the CTD Module 3. The course covers the general requirements for small molecules and biologics....

  • +4 months