PHARM Connect Congress is the largest and most important pharmaceutical and biotechnology business summit in the Central Eastern European region, taking place annually in March. With its 500+ participants from over 25 countries in the region and beyond, the Congress – to be held for the tenth time on 10-11 March 2020 – is a great platform to benchmark and network with an exclusive group of senior peers. We are here to help and accelerate the effectiveness of your marketing strategies, maximise ROI and stay ahead of the competition.
PHARM Connect Congress
PHARM Connect One-to-One interview with Terry Siggins, GE IP
UP-TO-DATE MARKET INSIGHTS
In order to ensure the quality of the conference programme, we work closely together with leading local and regional associations, European and global media partners and our Programme Advisory Committee, whose members are well-known pharmaceutical and biopharmaceutical industry experts of leading international companies. The conference programme offers the most up-to-date market insights into research and development, production, engineering, supply chain and quality management related topics.
Our event presents a unique opportunity to establish and develop fruitful, long-term and valuable business relations. Leading service providers of the pharmaceutical and biotechnology sector – covering a wide range of profiles from API’s and contract manufacturing to processing, biopharma solutions, biopharmaceuticals and biologicals, drug delivery systems, clean rooms, laboratory equipment, monitoring & inspection systems, quality control, packaging and labelling, automation, plant engineering and maintenance, logistics, cold chain storage and distribution, warehousing and many others – have the opportunity to meet the key decision makers of their targeted companies.
RETURN ON INVESTMENT
At TEG, we understand how challenging it is to find the right person, from each company at a time when they are ready to invest.
We are experts in supporting companies to increase their ROI, reducing sales cycles and accelerating the time-to-market.
PHARM Connect invites only senior decision makers with a purchasing power who are looking to invest into new services and solutions.
FIELD SEGMENT MANAGER – AUSTRIA
HEAD OF GLOBAL BUSINESS DEVELOPMENT - USA
Dr Erik Bogsch
HEAD OF BIOTECHNOLOGY R&D DIVISION - HUNGARY
EXECUTIVE SALES MANAGER EXPORT - ITALY
ITS BUSINESS PARTNER, SENIOR EXPERT - HUNGARY
SALES DIRECTOR GLOBAL PHARMA SOLUTIONS - BELGIUM
Prof Dr Christoph Herwig
PROFESSOR FOR BIOPROCESS ENGINEERING - AUSTRIA
GLOBAL KEY ACCOUNT MANAGER - GERMANY
Dr Péter Kása
TECHNICAL SERVICE MANAGER EASTERN EUROPE - HUNGARY
AREA SALES MANAGER PHARMA SOLID - GERMANY
Dr Sergii Sur
REGULATORY AFFAIRS DIRECTOR - UKRAINE
HEAD OF PROCESSES & PRODUCTS QUALITY - CROATIA
Dr Csaba Szőke
OPERATIONAL EXCELLENCE DIRECTOR - HUNGARY
PROGRAMME ADVISORY COMMITTEE
Dr Erik Bogsch
Head of the Biotechnology R&D Division, Gedeon Richter
Dr Erik Bogsch is the Head of the Biotechnology R&D Division at Gedeon Richter Plc. He is responsible for leading the R&D effort in the development of GR's biosimilar pipeline. Gedeon Richter Plc. is engaged in the development and manufacture of both bacterial cell fermentation based and mammalian cell fermentation based biosimilar products. GR has R&D, analytical & manufacturing capabilities in multiple locations in Hungary & Germany.
Dr Bogsch, a Hungarian national, has a Natural Sciences degree from the University of Cambridge and a PhD in cell biology from the University of Warwick. Following a brief postdoctoral academic research career, he worked in the food industry for many years in R&D, Quality & Manufacturing roles in the UK, Hungary & Germany. He joined Gedeon Richter Plc. in 2012, as commissioning lead for GR's biotechnology factory in Debrecen, Hungary, before moving into his current role.
Site Head and Managing Director, GSK Biologicals Kft.
Chris is the Site Director at the GSK Biologicals Kft. Vaccine manufacturing facility in Gödöllő. He joined the site in 2015, after 5 years working in Italy and Germany with Novartis Vaccines. Before moving into the vaccines business, he spent several years working for Amgen in the United States on the manufacturing of various bulk biologics. Chris is a chemical engineer, who has spent his career working in manufacturing facilities with roles in Manufacturing, Validation, Project Management, and Manufacturing Sciences & Technology.
Dr András Ballagi
Dr Ballagi moved to Sweden shortly after completing his degree in Bioengineering. There he worked in the field of the diagnosis and molecular evolution of veterinary viruses at the Swedish Veterinary Institute. He received his PhD for his research on application of PCR for virus detection and analysis of viral outbreaks. Later he moved on to fermentation technology of recombinant microorganisms at the University of Uppsala. After almost 20 years in Sweden he returned to Hungary in 2006 and joined Gedeon Richter Plc. to lead the technology development for biosimilar medicine production using bacteria (E.coli) as well as mammalian (CHO) cells.
In 2014 he formed the Biotechnology unit in the newly established Pharmatech Model Laboratory (PML) at the Budapest University of Technology and Economics, where he is also holding an Honorary Professorship. Since November 2016 he responsible for the recombinant protein development and production of human diagnostic at the Diagon Ltd, Budapest.
Head of Operational R&D, Polpharma
Marek Cichocki has been working in pharmaceutical industry for 13 years. He is an R&D expert with special focus on solid oral dosage forms development and manufacturing. Marek’s professional specialization includes: formulation design, scale-up and technology transfer activities, process validation, and new manufacturing methods.
Marek started his career in 2005 in Pliva Kraków (Poland) where he was a Formulation Scientist. From the beginning of 2010 Marek spent almost 4 years at Synthon BV (The Netherlands) being responsible for the implementation of newly developed products at Contract Manufacturing Organisations. In February 2014 Marek joined Polpharma (Poland) and became Head of Formulation Development team. Currently he is holding a position of Head of Operational R&D and his main responsibilities are: post-approval product maintenance, technology transfers, R&D support for industrial operations and new technologies implementation.
Dr Piotr Lipiński
Global Quality Auditor, Audit & Compliance, Europe II, Novartis Technical Operations Quality
Piotr has over 12 years of experience in pharmaceutical companies. Currently he is a Global Quality Auditor in Novartis. Before he worked in pharmaceutical manufacturing sites as Quality Assurance Specialist, Qualified Person and Quality Systems Manager.
The experience includes particularly quality systems implementation, self-inspections, trainings and auditing of materials, products suppliers and service providers. Piotr has detailed knowledge in scope of all GxP rules with special focus on Good Manufacturing Practice and Good Distribution Practice.
Piotr is a PhD Eng. in scope of Technology of Chemistry. Additionally, he completed post-graduate studies in scope of Industrial Chemistry at Medical University of Gdansk. He was participating as well in numerous courses related to GMP aspects in pharmaceutical industry.
Head of Processes and Products Quality, Belupo Pharmaceuticals
Lenka is a Pharmaceutical Professional with a unique combination of pharmaceutical management experience and exceptional knowledge in the areas of the New Product Evaluation, Laboratory Operations, Pharmaceutical Analysis and Project Management. She has an extensive experience in pharmaceutical industry in Research and Development, Regulatory Affairs, Quality Assurance and Quality Control Environment as well as profound knowledge of TPB and FDA, EU and Croatian regulatory submission requirements.
Strong knowledge of GMP, GLP, ICH guidelines and Pharmacopoeia is inevitable part of Lenkas‘ professional skills. Lenka is currently Head of Processes and Products Quality for Belupo Pharmaceuticals Croatia. Prior to this work, she worked in several positions at Apotex Inc. Toronto, Ontario and Genpharm Inc. (now Milan Pharmaceuticals) in Etobicoke, Ontario. Lenka has published several publications, is member of Pharmaceutical Sciences Group, Toronto and Croatian Association for Quality.
Prof Dr Stane Srčič
Head of Pharmaceutical Technology Department, Faculty of Pharmacy, University of Ljubljana
Dr Stane Srčič is a Professor for Pharmaceutical Technology at the Faculty of Pharmacy, University of Ljubljana, Slovenia. His expertise is focused on solid oral dosage forms development and manufacturing and includes pre-formulation and formulation, new manufacturing methods and customized equipment. After PhD he spent as post doc at the University of Regensburg, and was/is acting as a visiting Professor at the University of Liverpool, Szeged and Sarajevo. He served for more than 10 years as an expert from Slovenia on EMA (London) in the Committee for drugs in veterinary medicines and was responsible for quality parts of the dossiers.
He published more than 150 papers and is holder of numerous patents and patents applications in EU, US, Russian Federation and India. He is strongly connected with domestic and foreign pharmaceutical industry and was leading a lot of different academia-industry projects.
His international collaboration on the education and research areas has been recognized and awarded with the honorary doctorate from the University of Szeged (Hungary).
Dr Sergii Sur
Regulatory Affairs Director, Arterium Corporation
Dr Sur has over 25 years of work experience in the pharmaceutical market, including 14 years in management positions. He received his PhD degree in Pharmacy and published approximately 100 scientific publications. Between 1993 and 1998 he was the Head of State Laboratory for Quality Control of Medicines at the Institute of Pharmacology and Toxicology at the Ukrainian Academy of Medical Sciences in Kiev.
Between 1998 and 2005 he worked for the Ukraine Ministry of Health, firstly as the Director of Central Laboratory for Quality Control of Medicines and since 2000 as the Deputy Chief Inspector for Quality Control of Medicines. Since 2005, Dr Sur has been in his current position responsible for the development of a functional strategy in R&D; the development and introduction of R&D business processes and structure; and the organisation of research, development and registration of new products.
Additionally, Dr Sur is a member of the International Federation of Pharmacists (FIP) and since 1998 has been an adviser on International Pharmacopoeia and Pharmaceutical Preparations and since 2002 also on Traditional Medicines for the WHO which is headquartered in Geneva.
István Király graduated from the Technical University in Budapest as a mechanical engineer. During his professional career he has filled several technical- and production-related management positions in different industries at large international companies such as General Electric, DANONE, Alcoa and GlaxoSmithKline.
These challenges allowed him to be involved in the implementation and operation of different management and quality systems such as ISO, HACCP, GMP, Toyota Production System, Six Sigma and Lean Sigma. In 2006 he joined GSK Vaccines and started his career in Gödöllő Manufacturing site. He held various senior management positions until he was appointed as Managing director of the site in 2011. In 2015 he was nominated to VP, Head of Operations of the legacy Novartis Vaccines sites, overseeing the industrial operations of those sites and also managing the integration of those newly acquired manufacturing units into GSK Vaccines industrial network.
In 2016 he was promoted to his current position as VP, Site Director Siena & Rosia Operations, Italy at GSK Vaccines. In 2018 István returned to Hungary, and joined Human BioPlasma Kft. (part of Kedrion Group) as Site Director.
Dr Devendra Ridhurkar
Expert Scientist -Modified Release Formulations, NeuraxPharm
Dr. Devendra Ridhurkar works as an Expert Scientist (Modified Release Formulations) at Neurax Pharm, Barcelona, Spain. In his capacity he is responsible for development of a value added, complex and modified release generic formulations for highly regulated market. He was associated with various reputed pharmaceutical companies like Egis Pharmaceuticals, Budapest, Hungary, Dr.Reddys Laboratories Hyderabad, IPCA Laboratories, Alkem Laboratories and Macleods Pharmaceuticals Mumbai, India. He has over 12 years of experience in formulation and development of complex, modified release and various generics (ANDA), 505(b)(2) products for the global market using different NDDS approaches and various platform technologies which includes hot melt extrusion (HME), gastroretentive drug delivery systems, nanotechnology and cyclodextrin complexation to name a few. He also worked on development of solid oral generic formulations for highly potent drugs (oncology). He is an expert in materializing the design of experiments (DOE); quality by design (QbD).He obtained his M.Pharm and Ph.D. degree in Pharmaceutics from Indian Institute of Technology, Banaras Hindu University, Varanasi, India.
He is a member of editorial board for various pharmaceutical Journals and has earned to his credit over 8 peer-reviewed papers in reputed international and national journals and 5 patents to his credit. He has been associated with various pharmaceutical bodies in India and abroad namely Indian Pharmaceutical Graduate Association (IPGA) and American Association of Pharmaceutical Scientists (AAPS). He has attended and delivered seminars and presentations at various national and international conferences.
Dr Aljoša Maglica
Product Steward Senior, Lek, Sandoz
Aljoša Maglica received his B. S. degree in Chemical Engineering from the University of Ljubljana and earned his Ph.D. in Nanoscience and Nanotechnology from Jožef Stefan International Postgraduate School in Ljubljana. Aljoša has more than 5 years of experience in the Nanoscience and Nanotechnology according to research projects and scientific improvements to the production scale.
At the beginning of 2011 he started his work in the sterile production - Lek Pharmaceuticals. As a Product Steward Senior he is responsible for regular production support, transfer of new product to the production and quality of parenteral drug products. In addition, his is also covering the lyophilization process.
Dr Gábor Rónaszéki
Director of Quality Management, Institute of Isotopes
Gábor has 10 years of experience in pharmaceutical industry, specialized in: live virus Liofilization, Scale-up and Technology transfer, Process validation, Project Management, R&D support for industrial operations and new technologies, QM systems implementation. Currently he is Quality Systems Director at Institute of Isotopes Co. Ltd.
PhD Eng. in scope of genetic engineering, biotechnology including fermentation of recombinant microorganisms, protein purification, enzyme bioreactors. He obtained MBA degree at Rochester Institute, University of Buffalo USA and Budapest University of Technology and Economics, studying strategic management. He is co-author of a GMP guideline of food industry edited by Campden & Chorleywood Institute.
He worked as management representative in Healthcare sector with Fresenius. He worked also in food industry as Global R&D, Quality vice president in India, Hungary and Belgium obtaining experince in HACCP, GMP, Toyota System, lean manufacturing. He worked for TüV Süddeutsch as lead auditor of ISO 9001, 14001, 22000.
Plant Manager, Tchaikapharma High Quality Medicines INC
Vasil has over 14 years of experience in the field of pharmaceutical business. Currently he is the production manager at Tchaikapharma High Quality Medicines INC.
Vasil also gained experience as technical supervisor, operator, shift manager, plant manager and regional production manager.
As the regional production manager he is currently administrating the workflows between all local production shops and is responsible for the supply chain management, new projects management and the local business development.
His experience includes implementation of innovative technologies, e.g. Vasil implemented a new type of robotized blister feeding system and increased the production speed by 45 % , vastly decreased the start up time and the time for cleaning and also reduced the final products cost. He also implemented a special design serialization project, based on specific internal requirements and technological restrictions.
Violeta Dinić Milisavljević
Head of the Production Department, Alkaloid D.O.O.
Violeta has been working in the generic pharmaceutical industry for 16 years. She started her career as an R&D researcher, working on the solid dosage formulation and production process development, technology transfer and process validation for seven years. Currently, she is the Head of the Production Department of the production plant of Alkaloid AD in Serbia.
Violeta graduated from Ss. Cyril and Methodius University of Skopje - Faculty of Pharmacy (bachelor degree and specialisation on Pharmaceutical technology) and University of Belgrade - Faculty of Pharmacy (specialisation for QP). She is skilled in production planning, GMP, validation and regulatory issues.
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