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All results for portal tecnológico · 2315 results

ICH Q10: How to manage your Quality System including Quality KPIs - EU edition MasterClass

ICH Q10: How to manage your Quality System including Quality KPIs - EU edition MasterClass

12 - 13 December, 2022

Online Event

The ICH Q10 guideline - Pharmaceutical Quality System (PQS) - is one of the most important international regulations adopted by major regulatory bodies such as FDA, EMA, and others being cited in countless audit observations. The Master Class is completed by fundamentals of an appropriate Quality Culture which constitute the basis for a successful PQS....

  • +4 weeks
Particle Size Characterization - EU edition MasterClass

Particle Size Characterization - EU edition MasterClass

05 - 08 December, 2022

Online Event

This course will explores various approaches to particle size and shape characterization requirements for active pharmaceutical ingredients (APIs) during oral solid dosage product development....

  • +1 month
Advanced Pharmaceutical Quality Control - EU edition MasterClass

Advanced Pharmaceutical Quality Control - EU edition MasterClass

28 - 29 November, 2022

Online Event

The coursewill provide an update on the current state of the art of analytical development, validation and life cycle management of analytical procedures...

  • +1 month
Contamination Control Strategy - EU edition MasterClass

Contamination Control Strategy - EU edition MasterClass

24 - 25 November, 2022

Online Event

 This online course will present you what is meant by “Contamination Control Strategy”? It is a complex system of measures designed to minimize the risk of contamination in the manufacture of pharmaceuticals....

  • +1 month
Method Validation and Transfer with focus on the new ICH Q2(R2) MasterClass

Method Validation and Transfer with focus on the new ICH Q2(R2) MasterClass

05 December, 2022 - 05 December, 2022

Online Event

The new draft ICH guideline for method validation ICHQ2(R2) has been published for comment. Together with the new ICHQ14 guideline for method development, both guidelines represent a fundamental change of direction in method development and validation, e.g. implementation of ATP (analytical target profile). The WHO guidelines on transfer of technology in pharmaceutical manufacturing as well as the new draft ICH guidelines represent the new basis ...

  • +1 month
Reliable LPG gas cylinder filling scales for LPG bottling plants.

Reliable LPG gas cylinder filling scales for LPG bottling plants.

For a LPG gas filling station,it is very important and necessary to have reliable,durable and easy operation gas filling equipement. XiangKang is a technology company,concentrate on R&D,manufacture and sales of LPG gas filling machines for more than 20 years. In China,more than 60% gas station use our LPG gas filling scales.For oversea markets,the gas filling machines have been widely used in LPG gas filling station or gas service station,t...

Article

  • +1 week
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....

  • +1 month
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...

  • +1 month
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 ...

  • +1 month
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....

  • +1 month
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....

  • +1 month
Basic Principles of Computerized Systems Compliance Using GAMP® 5 Version 2 - EU edition MasterClass

Basic Principles of Computerized Systems Compliance Using GAMP® 5 Version 2 - EU edition MasterClass

21 - 22 November, 2022

Online Event

With modern facilities, installations, and equipment, PLCs and computers are an integral part of such systems. More often than not PLCs and computers are considered autonomous systems and handled separately within the QMS and protocols. In this two-day course, we will look at Basic Principles of Computerized Systems Compliance using ISPE’s GAMP5 Version 2 industry guidelines, compared to FDA’s Title 21 CRF Part 11 regulations, and EU’s Eudr...

  • +1 month
Pharma/Biotech Mergers and Acquisition MasterClass US

Pharma/Biotech Mergers and Acquisition MasterClass US

15 - 18 November, 2022

Online Event

Pharmaceutical Industry mergers and acquisitions are complicated, time-consuming, and challenging. No matter how big or small, there will always be legal, financial, and regulatory implications to consider as well as quality and safety, and Intellectual property considerations that must be addressed. This online training event will address the particular issues which affect Pharmaceutical M&A work, equipping participants with a broader understan...

  • +1 month
2nd Edition of Virology World Conference

2nd Edition of Virology World Conference

21 - 22 June, 2023

RM, Italy

Magnus Group is thrilled to invite you to its “2nd Edition of Virology World Conference” (VIROLOGY 2023) slated on June 21-22, 2023  in Rome, Italy. This premier event enlightens on the theme “Combating Global Pandemics through Virology Research & Innovations.” This virology summit will be highlighting recent advancements and technologies currently in use as well as those being developed on futuristic technologies for further viru...

  • +6 months
6th Annual Congress on Polycystic Ovarian Syndrome and Fertility

6th Annual Congress on Polycystic Ovarian Syndrome and Fertility

20 - 21 February, 2023

Amsterdam, Netherlands

The 6th Annual Congress on Polycystic Ovarian Syndrome and Fertility will be held in Amsterdam, the Netherlands, on February 20-21, 2023. It is a great pleasure to welcome all the researchers of their individual work on PCOS, scholars, and it is an extraordinary opportunity to go to this meet that investigates the information about the turmoil of PCOS and it is an exceptionally awesome benefit to have key speakers who will investigate their...

  • +6 months