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 firstname.lastname@example.org or call +44 (0)207 036 1300.
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.
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 report covers topics including investigating continuous bioprocessing, flexibility in single-use systems, and the need to seek new products from suppliers.
View the report now - Click 'Download' on the right >>
Key Findings Include:
- 43% of respondents indicated that technology is the main hindrance in achieving continuous processing
- Sustainability in disposable solutions is extremely important to manufacturers - on a scale of 1-10 (10 being most important), sustainability was ranked 7.5.
- The majority of manufacturers actively search for new technologies and solutions every 6-12 months
Click Download on the right to view the report now >>
Polymer-based single-use systems from Parker Prädifa offer major benefits in biopharma production over conventional steel- and glass-based multi-use solutions: They can reduce the risk of leakage or malfunctions of container closure systems and thus mitigate the risk of contamination. Through a wide range of available container sizes, a scalable production environment can be achieved. In addition, customizing SUS to meet the specific needs of the application environment and tailoring it to fit an existing, validated production framework has significant potential for cutting capital expenditures and overall system costs.
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.
Sampling is a requirement in every process step of biopharmaceutical manufacturing, with an increasing demand on accuracy the closer it comes to final finish. Avantor´s infographic demonstrates a 4-step process to develop a highly efficient and accurate sampling system, covering product conceptualization considerations, engineering design and proof of concept, Quality by Design and final production and manufacturing.
Implementation of single-use powder delivery systems in continuous biopharmaceutical manufacturing processes: A case study from Avantor
Single-use technologies have seen impressive progress over the last decade, but there are still significant needs for these technologies to be applied in upstream and downstream processes. The infographic will give an insight on the advantages of implementing a single-use powder delivery system in the continuous manufacturing process and shows a case-study for delivering exact quantities of clump free material for the delivery of buffer prep materials.
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.
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.
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