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SAE Media Group announces the return of the 7th Annual Lyophilisation Conference taking place on the 3rd and 4th June 2019, in London, UK.


Lyophilisation (or freeze drying) remains one of the most exciting and rapidly advancing technologies in the pharmaceutical industry to date. By 2020, the lyophilisation equipment market is projected to exceed 8% CAGR reaching approximately £4.4 billion. With up to a third of all FDA-approved parenterals and almost half of all injectables expected to be lyophilised in the near future, significant strides toward better standards and regulation are also anticipated to follow suit.


Despite being a relatively old process, lyophilisation continues to raise challenges in conjunction with ever changing biopharmaceutical products that carry their own set of inherent complexities. Join us along with key opinion leaders from all areas of pharmaceuticals and biologicals to explore formulation science, materials characterisation, novel and alternative technologies, mathematical modelling and regulatory updates. 


 

Participating in this year’s Lyophilisation 2019 conference provides a chance to connect with research and industry leaders with the aim of tackling the most pressing hurdles in multiple areas of interest within lyophilisation:
 

  • Scrutiny of product complexity via material characterisation with the intention of gaining a deeper understanding of formulation design and its development.
  • Assessing the essential factors and fitting mechanical investment for successful scale up and tech transfer
  • Utility of appropriate process analytical technology tools for process monitoring, optimisation and lyophilisation cycle development
  • Conducting accurate modelling and estimation for prediction and risk reduction.
  • Exploring developing technologies and alternatives to traditional lyophilisation techniques

VPs, Directors, Chiefs, Heads, Principals, Managers and Analysts of:

  • Lyophilisation/Freeze-drying
  • Formulation Scientists
  • Principal Scientist
  • Process Development/Engineer
  • Sterile/Fill-Finish
  • Production
  • PAT
  • CMC
  • Chemistry
  • Manufacturing
  • Quality Assurance/QA

Amatisgroup; Arlenda; Aznil Telstar Technologies, SLU; Abbott Healthcare Products BVá; BioNTech; Baxter SA; Bayer A G; Biofire Diagnostics; Biopharma Group; BioPharma Technology; Boehringer Ingelheim; Boehringer-Ingelheim; Bristol-Myers Squibb; BSP PHARMACEUTICALS Srl; BUCHI UK Ltd ; DeMontford University; DSM; Ferring Pharmaceuticals A/S; Fresnius Kabi Austria GmbH; F. Hoffman-La Roche Ltd.; GEA Process Engineering; Genzyme Ireland Ltd; GlaxoSmithKline; GlaxoSmithKline plc; GSK; GSK Manufacturing S.p.A.; Hosokawa Micron BV; Imperial College London; LFB Technology; INDATECH SAS; Janssen Pharmaceutica NV; MedImmune; MedImmune Inc.; Merck KGaA; Mylan; NIBSC; Novo Nordisk; OPTIMA pharma GmbH; Pacifi Ltd; Pfizer Inc; Pliva Croatia Ltd; RheaVita BV; Roche; Roche Pharmaceuticals; Sandoz GmbH; Syngenta Limited; TEVA Pharmaceuticals; University College Cork (UCC); University Of Central Lancashire; University of Ghent; Vetoquinol SA; Xellia Pharmaceuticals ApS;

Conference agenda

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8:30

Registration & Coffee

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9:00

Chairman's Opening Remarks

Xiaodong Chen, Senior Research Investigator , Bristol-Myers Squibb

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9:10

Recent advances in technologies and approaches in freeze-drying: a quick tour

Kevin Ward, Director of Research and Development, BioPharma Technology

• Formulation characterisation – freeze-drying microscopy and thermal analysis
• Process monitoring and control – PAT and controlled nucleation methods
• Approaches, limitations and practicalities in scaling up the freeze-drying process
• Post-lyophilisation testing – new technologies for understanding the final product
 

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9:50

Anatomy of the Lyophilization Process: Considerations for a Successful Tech Transfer

Anthony Cannon, Regional Director, ExM, GTO Bio/Sterile European Region, MSD

• Tech transfer of a lyophilized product
• Overview of the lyophilization process and the critical process parameters
• Specific focus on the technical considerations with analysis of the impact on the lyophilization recipe
• Impact of deviations to the CPPs on the product quality during transfer activities
 

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10:30

Morning Coffee

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11:00

Representative Scale-down Lyophilization Cycle Development Using a Micro Freeze-Dryer

Xiaodong Chen, Senior Research Investigator , Bristol-Myers Squibb

A scale-down lyophilizer was used to simulate at-scale lyophilization development and optimization. Equivalent lyophilization performance between the scale-down lyophilizer and a laboratory lyophilizer were demonstrated for placebo and mAb drug products. By changing the MicroFD® Kv, laboratory, and potentially manufacturing cycles, may be simulated using this lyophilizer for tremendous API savings:
• The MicroFD® is designed with precision machined, temperature controlled aluminium blocks that make direct contact with the outer vials. These blocks are designed to mimic vial-to-vial contacts that control inter vial heat transfer
• Demonstrated the ability to fine-tune the MicroFD® heat transfer coefficient (Kv) to match the Kv of vials in a Lyostar III laboratory scale unit
• The resulting performance between scales results in equivalent product primary drying times, product temperature profiles, and critical quality attributes (CQAs)
• A workflow is proposed using the scale-down lyophilizer to simulate at-scale lyophilization development and optimization. 

 

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11:40

Preventing Cross Contamination during Lyophilization

Richard Denk, Head Sales Containment, SKAN AG

•  What are highly potent/toxic Biopharmaceutical Products
•  What are the GMP and Occupational Safety Requirements
•  How to prevent Product Contamination during loading the Lyo
•  Cleaning Requirements and Occupational Safety Requirements
 

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12:20

Networking Lunch

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13:20

A proposed scientific rationale for the establishment of acceptance criteria for leak rates in pharmaceutical freeze dryers

Aled Jones, Manufacturing Support Manager, Ipsen Biopharm Ltd.

• A methodology has been developed to determine the theoretical quantity of air that could leak into a pharmaceutical freeze dryer based on vacuum pressure increase.
• Based on the potential maximum bioburden and particulate level of the leaked air from potentially unclassified areas, simple calculations can be undertaken to determine the maximum allowable leak rate that will still maintain Class 100 / Grade A conditions for the duration of the lyophilisation cycle.
• It will be shown that the 2 x 10-2 mbar-litre/sec specification, that is frequently quoted as the acceptable leak rate for modern pharmaceutical freeze dryers may not be appropriate to maintain Grade A conditions for freeze dryers of differing volumes with lyophilisation cycles of differing lengths.
• This methodology can then be used as a justification for the setting of leak rate limits for new cycles or freeze dryers based on potential microbial risk rather than equipment process capability. 

 

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14:00

Application of Infrared Thermography and Multivariate Image Analysis for the on-line Monitoring of a Freeze-Drying Process

Davide Fissore, Professor, Politecnico Di Torino

• Infrared camera, placed inside a freeze-dryer, can be used to monitor product temperature in several vials, in different positions.
• Product temperature measurement may be used to infer the residual amount of ice in the primary dying stage, as well as the parameters of a simple one-dimensional model of the process.
• The system may be used also to track the evolution of the product in the freezing stage.
• Using Multivariate Image Analysis (MIA) it becomes possible to extract additional information about process dynamics.
• The proposed MIA-based PAT system is able to efficiently detect undesired events occurring during the process.
• Information obtained through a standard RGB camera may be also include in the PAT system.
 

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14:40

Afternoon Tea

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15:10

Optimisation of industrial freeze-drying cycle - Two real life examples

Mostafa Nakach, Head of Pharmaceutical Engineering Group, Sanofi-Aventis R&D

• Comparing two dated lyophilized products (60’s) with historical cycles that exhibit distinct complications
• Development and optimization of manufacturing processes to overcome the lack of physical chemistry data from dated products
• Applying product knowledge, new freeze dryer knowledge, simulation and process modelling
 

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15:50

In silico evaluation of intermolecular interactions in the pharmaceutical formulations during freeze-drying processes

Mire Zloh, Honorary Professor, University of Hertfordshire

• In silico methods can predict intermolecular interactions between components of pharmaceutical formulations.
• A combination of molecular docking and molecular dynamics simulations methods provides insights into the protective effects of formulations on a molecular level.
• Such information can guide the computer aided development of future formulations. 

 

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16:30

Chairman’s Closing Remarks and Close of Day One

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8:30

Registration & Coffee

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9:00

Chairman's Opening Remarks

Sune Klint Andersen, Principal Scientist Spray Drying , Janssen Pharmaceutica NV

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9:10

Low Temperature Drying Processes for Biopharmaceuticals

Sune Klint Andersen, Principal Scientist Spray Drying , Janssen Pharmaceutica NV

• Challenges in drying of biopharmaceuticals
• Drying process landscape and trends
• Emerging low temperature drying processes
 

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9:50

Primary Drying endpoint determination

Bert Van Meervenne, Senior Principal Scientist, Pfizer Manufacturing

• Overview & discussion of different tools to determine primary drying endpoint
• Pros and Cons of each method
• Touching briefly additional potential of these tools
 

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10:30

Morning Coffee

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11:00

Applications for Impedance Spectroscopy in the Determination of In-Vial Phase Behaviour

• Through Vial Impedance Spectroscopy – An Introduction
• Dielectric loss mechanisms in frozen solutions
• Measurement frequency selection for different facets of the freezing process (ice nucleation to solidification end point)
• Determination of in-vial glass transitions and collapse phenomena

 

Geoff Smith, Professor of Pharmaceutical Process Analytical Technology, DeMontfort University

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11:40

Formulation for freeze drying, development and applicability

Paul Matejtschuk, Principal Scientist & Section Head, Standardisation Science, NIBSC

Increasing complexities of myriad pharmaceutical products and materials demand improved and novel methods that characterise and consequently provide essential information to support formulation design.
• How does freeze drying impact bio activity?
• Role of Design of Experiments in formulation development
• Using PAT tools - through vial impedance as an example

 

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12:20

Networking Lunch

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13:20

Long-Term Storage Stability and Effect of Moisture Content on Freeze-Dried Immunoglobulin G (IgG)

Daryl Williams, Director of Development, Chem. Eng. Discovery, Imperial College London

• High protein concentration products for targeted therapeutic use are commonly manufactured by freeze-drying. 
• The long-term storage stability of freeze-dried plasma derived Immunoglobulin G (IgG) from moderate to high concentrations (1, 5, 10 and 20 % w/v) was assessed for -20°C, 20°C, 45°C
• At -20°C < 1% of monomer loss, 20C <5% monomer loss, whilst 45°C a 15%-39% decrease in monomer concentration
• Moisture content in vial effected formulation stability
 

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14:00

Assessment of Aggregation in Lyophilised Biologics

Paul Barry, Development Scientist, Sanofi

• Using large data sets to identify common cause(s) for aggregation occurrence.
• Analytical assessment of aggregation
 

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14:40

Current state of MTM – True PAT with high future potential

Georg Frinke, Process Engineer, Bayer AG

• Current state of MTM Technology
• Operating principle
• Future potential & Limitations

 

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15:20

Chairman’s Closing Remarks, Afternoon Tea and Close of Day Two


Manufacturing Support Manager
Ipsen Biopharm Ltd.
Regional Director, ExM, GTO Bio/Sterile European Region
MSD
Senior Principal Scientist
Pfizer Manufacturing
Director of Development, Chem. Eng. Discovery
Imperial College London
Professor
Politecnico Di Torino
Professor of Pharmaceutical Process Analytical Technology
DeMontfort University
Process Engineer
Bayer AG
Director of Research and Development
BioPharma Technology
Honorary Professor
University of Hertfordshire
Head of Pharmaceutical Engineering Group
Sanofi-Aventis R&D
Development Scientist
Sanofi
Principal Scientist & Section Head, Standardisation Science
NIBSC
Head Sales Containment
SKAN AG
Principal Scientist Spray Drying
Janssen Pharmaceutica NV
Senior Research Investigator
Bristol-Myers Squibb

Exhibitors

Supporters

Workshops

From Physical Properties to Lyophilised Product
Workshop

From Physical Properties to Lyophilised Product

Holiday Inn Kensington Forum
5 June 2019
London, United Kingdom

VENUE

Holiday Inn Kensington Forum

97 Cromwell Road , London, United Kingdom

Holiday Inn Kensington Forum is perfectly situated in one of London’s most luxurious and beautiful areas within South Kensington. 

The hotel is just 2 minutes walk from Gloucester Road tube station for convenient travel to Hyde Park, London Eye, Tower Bridge plus more of London’s top attractions. There are also easy and direct links to some major transport hubs including Victoria, Kings Cross St Pancras, Paddington and Heathrow. 

This distinctive hotel in south London has so much to offer to make all guests really feel at home. The latest Holiday Inn relaunch is not just about the new look and feel for the hotel but to offer guests more benefits during their stay including a pillow menu for extra comfort during their sleep and a curved shower rail for more spacious feel. 

In addition to our 906 rooms, all business guests can take advantage of our meeting and conference facilities including High Speed Internet Access and unlimited Starbucks coffee at The Academy. Our hotel’s professional event planners are on board to help take the hard work and stress away from planning your next event. 

So whether you in London on business or pleasure, make the Holiday Inn London Kensington Forum your first choice of hotel and book your accommodation for our lowest internet rate guarantee. 

A number of our clients have been approached by third party organisations offering to book hotel rooms. We would advise that you do not book through them as they are not representing the SMi Group. SMi Group books all hotel rooms directly. If you are approached by a third party organisation then please contact us before making any bookings. If you have already booked a hotel room using a third party organisation, we would highly recommend contacting the hotel you were booked into to ensure a booking has been made for you. We would also advise you to please check the terms and conditions of the booking carefully.
HOTEL BOOKING FORM

Lyophilisation 2019 Attendee List

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Interview with Geoff Smith, De Montfort University

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Speaker Interview with Xiaodong Chen, Bristol-Myers Squibb

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In silico approaches to aid rational design of freeze dried formulations

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Lyophilisation 2019 Full Programme

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Lyophilisation 2019 Workshop Programme

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Lyophilization of an Oral Anti-Viral Agent

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Humidity Induced Collapse in Freeze Dried Cakes: A Direct Visualization Study using DVS

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Snap Shot of Attendees at Lyophilisation 2018

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Lyophilisation 2019 Speaker Line Up

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Lyophilisation 2019 Conference Brochure

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Exhibitors


Testo

Exhibitors
https://www.testo.com/en-UK/

The validation of sterilization and freeze-drying processes is a key element of your quality assurance and shows the high level of safety of the products you make. With our testo 190 CFR data logger system, we support you according to your needs in terms of fulfilling all regulatory requirements in a highly efficient way.

Media Partners


Lyophilization World

Supporters
https://www.lyophilizationworld.com/

Lyophilization World is a global platform in the field of lyophilization and freeze drying technology. Follow us to be informed in a unique way about current solutions, future trends and news in lyophilization


pharmanews hq

Supporters
http://http://pharmanewshq.com

MedChemNet provides a unique and unparalleled platform for the medicinal chemistry community to share insights, discuss the latest research, and help move the field forward. MedChemNet covers all aspects of the drug discovery pipeline, from target identification and validation, through computer aided drug design (CADD), synthesis, screening and other biophysical techniques, to development of novel lead compounds and pre-clinical in vivo proof of concept. We also cover the design of synthetic drug delivery carriers and ADME/toxicology studies, as well as intellectual property and economic related issues. Website: Welcome to Pharma News HQ, the journal dedicated to the pharmaceutical and biopharmaceutical contract services. With regular sections on contract manufacturing, contract research, contract packaging, formulation/development services, contract analytical testing, APIs, stability testing, clinical research and other areas, we bring the most complete coverage of trends and issues in the industry. Pharmanewshq.com is the only website focusing specifically on issues relevant to pharmaceutical professionals working with technology, be it development, engineering, IT or production.


Pharmaceutical Technology

Supporters
http://www.pharmaceutical-technology.com

Pharmaceutical-technology.com is the only website focusing specifically on issues relevant to pharmaceutical professionals working with technology, be it development, engineering, IT or production. Pharmaceutical-technology.com brings you the latest in industry projects and updates, along with the news, views and trends that leading professionals – from senior executives to manufacturing managers and heads of procurement – require to stay on top of their field.


World Pharma News

Supporters
http://www.worldpharmanews.com/



IPI

Supporters
http://www.ipimediaworld.com

IPI – International Pharmaceutical Industry Established by professionals with over 30 years experience in the Pharmaceutical and Life sciences publishing sectors. We have identified the needs of these dynamic industries, and have listened carefully to our readers and advertisers. With strong collaboration between Pharmaceutical and Life sciences Industry Associations we have created a global distribution network. We give you a promise to become a reliable extension of your marketing and communication arm. If necessary we will integrate our expertise with your needs. Incorporating new and innovative communication methods we will help to highlight your expertise.


pharmaphorum

Supporters
http://www.pharmaphorum.com

pharmaphorum drives innovation within the pharmaceutical industry, by bringing healthcare together through a suite of media services that help produce and disseminate thought leadership, combined with an online platform for communicating messages to a global audience.Visit www.pharmaphorum.com


Drug Discovery Today

Supporters
http://www.drugdiscoverytoday.com/

Drug Discovery Today covers the whole of the preclinical drug discovery process. The reviews are cutting edge, written by experts in their respective fields and cover all aspects of drug discovery from genomic and proteomic approaches, computational drug design, medicinal chemistry and the translation of these sciences to therapies.


Pharmalicensing

Supporters
http://www.pharmalicensing.com

Pharmalicensing (www.pharmalicensing.com) is the premier biopharmaceutical Open Innovation resource designed for professionals involved with partnering, licensing and business development worldwide. Actively supporting all forms of partnering and in- and out-licensing activities, Pharmalicensing utilizes the unique online Showcase Profiling & Discover services, as well as its renowned Partnering Search service leveraging its global network of industry experts, to enable companies to identify and engage with appropriate partners around the world. Pharmalicensing is actively utilized by many tens of thousands of industry professionals each month. Pharmalicensing is a division of Cognis Group, Inc.

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Holiday Inn Kensington Forum

97 Cromwell Road
London SW7 4DN
United Kingdom

Holiday Inn Kensington Forum

Holiday Inn Kensington Forum is perfectly situated in one of London’s most luxurious and beautiful areas within South Kensington. 

The hotel is just 2 minutes walk from Gloucester Road tube station for convenient travel to Hyde Park, London Eye, Tower Bridge plus more of London’s top attractions. There are also easy and direct links to some major transport hubs including Victoria, Kings Cross St Pancras, Paddington and Heathrow. 

This distinctive hotel in south London has so much to offer to make all guests really feel at home. The latest Holiday Inn relaunch is not just about the new look and feel for the hotel but to offer guests more benefits during their stay including a pillow menu for extra comfort during their sleep and a curved shower rail for more spacious feel. 

In addition to our 906 rooms, all business guests can take advantage of our meeting and conference facilities including High Speed Internet Access and unlimited Starbucks coffee at The Academy. Our hotel’s professional event planners are on board to help take the hard work and stress away from planning your next event. 

So whether you in London on business or pleasure, make the Holiday Inn London Kensington Forum your first choice of hotel and book your accommodation for our lowest internet rate guarantee. 

HOTEL BOOKING FORM

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WHAT IS CPD?

CPD stands for Continuing Professional Development’. It is essentially a philosophy, which maintains that in order to be effective, learning should be organised and structured. The most common definition is:

‘A commitment to structured skills and knowledge enhancement for Personal or Professional competence’

CPD is a common requirement of individual membership with professional bodies and Institutes. Increasingly, employers also expect their staff to undertake regular CPD activities.

Undertaken over a period of time, CPD ensures that educational qualifications do not become obsolete, and allows for best practice and professional standards to be upheld.

CPD can be undertaken through a variety of learning activities including instructor led training courses, seminars and conferences, e:learning modules or structured reading.

CPD AND PROFESSIONAL INSTITUTES

There are approximately 470 institutes in the UK across all industry sectors, with a collective membership of circa 4 million professionals, and they all expect their members to undertake CPD.

For some institutes undertaking CPD is mandatory e.g. accountancy and law, and linked to a licence to practice, for others it’s obligatory. By ensuring that their members undertake CPD, the professional bodies seek to ensure that professional standards, legislative awareness and ethical practices are maintained.

CPD Schemes often run over the period of a year and the institutes generally provide online tools for their members to record and reflect on their CPD activities.

TYPICAL CPD SCHEMES AND RECORDING OF CPD (CPD points and hours)

Professional bodies and Institutes CPD schemes are either structured as ‘Input’ or ‘Output’ based.

‘Input’ based schemes list a precise number of CPD hours that individuals must achieve within a given time period. These schemes can also use different ‘currencies’ such as points, merits, units or credits, where an individual must accumulate the number required. These currencies are usually based on time i.e. 1 CPD point = 1 hour of learning.

‘Output’ based schemes are learner centred. They require individuals to set learning goals that align to professional competencies, or personal development objectives. These schemes also list different ways to achieve the learning goals e.g. training courses, seminars or e:learning, which enables an individual to complete their CPD through their preferred mode of learning.

The majority of Input and Output based schemes actively encourage individuals to seek appropriate CPD activities independently.

As a formal provider of CPD certified activities, SAE Media Group can provide an indication of the learning benefit gained and the typical completion. However, it is ultimately the responsibility of the delegate to evaluate their learning, and record it correctly in line with their professional body’s or employers requirements.

GLOBAL CPD

Increasingly, international and emerging markets are ‘professionalising’ their workforces and looking to the UK to benchmark educational standards. The undertaking of CPD is now increasingly expected of any individual employed within today’s global marketplace.

CPD Certificates

We can provide a certificate for all our accredited events. To request a CPD certificate for a conference , workshop, master classes you have attended please email events@saemediagroup.com

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