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Download the Agenda | Disposable Solutions for Bio Manufacturing

Download the Agenda | Disposable Solutions for Bio Manufacturing

18th – 20th February 2020, Leonardo Royal Hotel Berlin Alexanderplatz, Berlin, Germany

Your 3 day programme is designed to guide you through your journey

SYSTEM IMPLEMENTATION: Develop seamless implementation strategies to boost manufacturing capabilities.

SYSTEM MANAGEMENT: Benchmark and overcome your management challenges, ensuring you are maximising your facility!

FUTURE TECHNOLOGY: Remain at the forefront of innovation and most importantly, understand how you can maximise efficiencies. 

Our forum brings together 100+ senior industry experts and provides a platform to benchmark your technological adoption and process optimisation, as well as discover the industry’s newest technologies!

To view the full agenda and speaker sessions download the form to your right >> 

Don't like forms? contact enquire@iqpc.co.uk or call +44 (0)207 036 1300.

Behind the Scenes with Sanofi Pasteur: Extractables & Leachables Testing

Behind the Scenes with Sanofi Pasteur: Extractables & Leachables Testing

Pharma IQ spoke to Ken Wong - MTech/Process Technology - Extractables & Leachables Sanofi Pasteur, who has been leading the site’s E&L programme since he joined just over two years ago, to explore Ken’s real world projects at the pharma firm in regards to extractables and leachables testing.

Trends and Success Factors in Disposable Technologies and Single Use Systems for Biomanufacturing

Trends and Success Factors in Disposable Technologies and Single Use Systems for Biomanufacturing

In this benchmarking survey report Pharma IQ draws comparisons with previous survey conducted at the end of 2013. Find out what has changed in the industry, what to consider when choosing new suppliers, best way to tackle extactables & leachables and we compare different investment approaches.

7 Challenges of Implementing Single-Use Systems in Biomanufacturing

7 Challenges of Implementing Single-Use Systems in Biomanufacturing

In this interview Jerold Martin, Sr. Vice President, Global Scientific Affairs for Pall Life Sciences and Chairman of the Bio-Process Systems Alliance (BPSA), speaks about the aims of the PDA Technical Report Number 66, Application of Single Use Systems in Pharmaceutical Manufacturing and what progress has been made with standardising practices for disposables in biomanufacturing. Plus, he highlights seven challenges the industry will face in 2015 during the implementation of single-use systems.

Industry Overview

Industry Overview

Based on the opinions of over 50 biopharma experts, we have put together this industry overview discussing the latest drivers and challenges for the single-use market. This infographic covers topics including investigating continuous bioprocessing, flexibility in single-use systems, and the need to seek new products from suppliers. 

Infographic: Optimising Process Efficiency in Biomanufacturing

Infographic: Optimising Process Efficiency in Biomanufacturing

In today’s bioprocessing industry, there is a demand to cut manufacturing costs while maintaining product safety and quality; flexibility needs to be increased and time to market reduced. With insights from Dr Philipp Hess, Managing Partner at PHA and our recent industry survey, this infographic will cover the key elements of process optimisation and efficiency used in single-use technology solutions.


7 Simple Steps for Selling Your Single-Use Solution

7 Simple Steps for Selling Your Single-Use Solution

There are a number of important considerations that need to be made in order to maximise your chances of success in selling your solution. This handy guide provides an overview of the decision making process for solution adoption in single-use systems and the key steps that need to be taken to give your product the best chance of customer success.

This infographic includes information on:

- Identifying decision makers and the decision making unit

- Establishing  the scale of implementation for your customer

- Preparing your data to ensure it will pass SOPs, QA and validation procedures