Seminar

1-day seminar on Material Qualification

November 21, 2017

DOC will Sponsor the seminar organized by ELCHEMA Paliginis Bros in Athens, Greece on November 21, 2017.

 

Topic of the day will be “Glass, Elastomers, Plastics, Polymeric Material in Process Devices for Pharmaceutical Systems: Qualification Approach based on recent USP & EU regulation

 

Antonio Legnani, Technical & Validation director, and Federica Annovazzi, Project Manager, will share DOC experience in all aspects related to Material Qualification and Sterilizing Grade Filter Validation as ruled by the recently revised USP monograph and European regulation.

Focus will also be on the Qualification studies of in-process material (e.g. filters, tubing,..) as well as primary containers with the specific product formulation as it is becoming an increasing “hot topic” in EU as well in USA GMP Community.

 

Download the Seminar Program for additional information and subscription

 

 

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Masco Seminar in Ireland

25th May 2017

 

 

Masco Group is pleased to invite you to our Seminar, organized in collaboration with Steritech Ltd that will be held in Dublin on 25th of May 2017.

How to register: Please Contact Alf Gregg at: ag@steritech.co.uk

 

 

Regulatory update and Technology Innovation

15th of February 2017

 

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Masco Group is pleased to invite you to our Seminar, organized in collaboration with Melapack Kft. Process division dedicated to the Pharmaceutical and Cosmetic Industries.

Through the several lectures presented, it will be provided an update about the latest regulatory requirements and an anticipation about the ones that will become effective starting from 2017.

Moreover the latest technological trends related to the manufacturing of pharmaceutical and cosmetic finished products like sterile solutions, suspension and ointments will be shown through specific case studies coming from our experience.

The last part of the Seminar will be dedicated to the Quality matter and it will cover the qualification and validation aspects of material, equipment and containers in contact with the pharmaceutical drug formulation.

Entry is free, however places are limited, please register in advance to confirm your attendance.

For any additional information regarding the participation please fill the form below

 

 

 

EU GMP NEW APPROACH: Commissioning and Qualification

3rd and 4th of October 2016

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Masco is organizing a 2-day-Validation seminar, which will be held in St. Petersburg, 3rd – 4th of October 2016.

The topic of the event is the following: “EU GMP NEW APPROACH: Commissioning and Qualification”.

Please, find here the detailed program.

The seminar is focused on technical and regulatory aspects of validation of a pharmaceutical facility as per the latest EU GMP Annex 15 as well as NEW EP Monograph.

On October 4th a visit to “Polysan” factory (http://eng.polysan.ru/) is organized for all participants.

For any additional information regarding the participation please fill the form below