Pharmaceutical Industry Congress 2026
april 27-29, 2027
To the conference remains:
320 days 20 hours 9 minutes 23 seconds
Participate in industry events:








Conference room 1
Hall B
Your Laboratory: From Vision to a State-of-the-Art Turnkey Research Facility – A Multidisciplinary Design Symphony Driven by ALPBIS Group and KDM Group
ALPBIS Group: Turnkey Laboratories of Tomorrow – From Vision to Completion Labotech 2026 – ALPBIS Group, an expert in creating modern research spaces, is presenting a comprehensive model for managing laboratory projects at the Labotech trade show. The company offers a unique “from vision to turnkey implementation” approach, relieving the client of the burden of coordinating design and construction processes.
Key pillars of the ALPBIS Group’s offering:
· Design and consulting: Creating ergonomic and safe functional layouts compliant with standards.
· Custom-made equipment: Manufacturing and installation of certified laboratory furniture and fume hoods.
· Installations and equipment: Installation of specialized utility networks and delivery of advanced research equipment.
· Service and training: Full after-sales support, including warranty service and equipment calibration. “At the Labotech trade show, we want to demonstrate that building a laboratory doesn’t have to be a complicated process. Thanks to our experience, we guide the investor through every stage—from bare walls to a fully functional research center,” says the ALPBIS Group team.Based in Bielsko-Biała, the company remains a leader in the modernization of scientific and industrial infrastructure in Poland, thanks to its ISO certification and a broad team of experts.
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10:30 11:30
Roman Czykwin
Tomasz Siwik – Sales Director and Member of the Management Board of ALPBIS Group.
Your Laboratory: From Vision to a State-of-the-Art Turnkey Research Facility – A Multidisciplinary Design Symphony Driven by ALPBIS Group and KDM Group
1. Introduction: Architecture and Technology Under One Roof
· Welcome and introduction of speakers: experts from the ALPBIS Group (technology/equipment) and the KDM Group (architectural design/general contracting).
· Thesis: Building a laboratory is not just a “simple renovation”—it is an operation on a living organism.
2. Architectural Design: The Foundation for Science – KDM Group Panel
3. Industry Integration: Where Construction Meets Technology – Joint Discussion
4. Turnkey Implementation: From Shell to Sterility – ALPBIS Panel
5. Safety and Acceptance: Shared Responsibility
6. Summary and Q&A
Conference Organizer
NanoBioMedical Centre
Conference room 1
Hall B
Microplastics in Laboratory Analysis - Methodological and Regulatory Challenges
Microplastics in Laboratory Analysis - Methodological and Regulatory Challenges
Increasing regulatory requirements in the European Union, together with the rapid growth of environmental research, have made the analysis of microplastics one of the key challenges for modern laboratories. This discussion panel will focus on practical aspects of microplastic analysis, including sample preparation, polymer identification, detection limits, and the comparability of results between laboratories.The experts will also discuss issues related to method standardisation, laboratory accreditation, and the impact of emerging EU regulations, including the Drinking Water Directive, recent developments within the REACH regulation, and forthcoming environmental monitoring requirements. The panel will offer an opportunity to exchange perspectives and practical experience between researchers, manufacturers of analytical instrumentation, and testing laboratories.
NanoBioMedical Centre (CNBM), Adam Mickiewicz University (AMU), Poznań, is an interdisciplinary research centre focused on advanced studies of nanomaterials and biomaterials and their applications in medicine, biology, and modern materials technologies. Our mission is to develop cutting-edge nanotechnologies and biomaterials and to educate highly skilled specialists in materials engineering and nanobiomedicine.
CNBM combines state-of-the-art research infrastructure, expert knowledge, and an interdisciplinary approach to develop materials for key areas of modern medicine, including drug delivery systems, tissue engineering, biomedical diagnostics, and biosensors. The Centre is equipped with modern research facilities that support both the fabrication and comprehensive characterisation of functional materials. Its technological infrastructure includes a fully equipped chemical laboratory, 3D printing systems, ALD and CVD deposition systems, and electrospinning equipment, enabling the production of advanced materials with preciselycontrolled properties.
Our infrastructure is complemented by a wide range of advanced analytical instruments, including electron microscopes (SEM, TEM, HRTEM), atomic force microscopes (AFM), confocal microscopes (CLSM), X-ray diffractometers (XRD), as well as NMR and ICP-MS spectrometers. This combination of facilities allows us to carry out comprehensive materials research, from structural and physicochemical analysis to functional performance testing. This infrastructure also supports the development of solutions with strong application potential, extending beyond medicine to areas such as energy technologies and catalysis.As a scientific partner, CNBM actively supports collaboration between academia and industry, promoting innovative laboratory solutions, new research methods, and the effective transfer of knowledge and technology to real-world applications.
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11:45-12:05
Marta Woźniak-Budych, Centrum NanoBioMedyczne UAM
Introduction: An Overview of Microplastics

12:05 - 12:25
Jan Szczepański, WITKO Sp. z o.o.
Challenges related to microplastics
12:25 - 12:55
Bartłomiej Koźniewski, Pro-Environment Polska
Plastic detection equipment
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12:55 - 15:00
Prof. dr hab. Agnieszka Kamińska Instytut Chemii Fizycznej Polskiej Akademii Nauk
mg Jan Szczepański
dr inż. Bartłomiej Koźniewski
Open discussion
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14:00 - 15:00
Dominik Wójcik - Dyrektor i Wiceprezes IKA Poland
Viscosity measurements are key to selecting the right products. How to measure to ensure reliable results?
Why net calorific value is more important than gross calorific value in the context of emission limits and fees.
Laboratory 4.0 – safety and online equipment monitoring.
Conference Organizer
ohaus
Booth, Hall B , B4.20
Best practices for operating and maintaining centrifuges
Medal Ceremony
Date
6 maytime. 12:00
Location
Hall BTrade Fair Studio

10:30 - 11:00
Harry Pomfret - Haier Biomedical / FROST
ULT Freezer Care - Maintain Efficiency and Protect Your Samples
The lecture will be conducted in English

11:00 - 11:45
Tomasz Kasikowski – Kawa.ska
Life in 3D - What a Confocal Microscope Sees

11:45 - 12:00
Medbase Sławomir Kmak
Medbase - The Future of Evidence-Based Digital Pharmacotherapy It starts now!

12:00 - 12:30
Pharmalogics Mateusz Gołąb
What should be considered when approaching the research and development of medicinal products? Application types and CTD dossier perspectives.
12:30 - 13:15
Science Pharma Joanna Pawlak
The pathway from drug candidate to obtaining market authorization: a regulatory roadmap.

13:15 - 13:35
Filip Maciąg - MetaSystems
Automated microscopy solutions for routine diagnostics labs and more

13:35 - 14.00
Sołtysiński Kawecki & Szlęzak Katarzyna Wójcik-Welc
Pharmacy Advertising and the Law: Where Is the Line Between Informing and Prohibited Promotion? Upcoming Legislative Changes.

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14:00 - 15:00
Arche Consulting Mikołaj Król
Artur Nycz
Life Sciences Recruitment Behind the Scenes: Trends and Realities of the Competition for Doctors, Pharmacists, and Pharmaceutical Market Experts.

15:00 - 15:30
GRUPA4 Jakub Woźniak
European Funds for Biotechnology and Pharmaceutical Companies – What Can You Apply for and How to Secure a Grant in 2026?

15:00 - 15:30
Sylwia Kunca –Sylwia Kunca – chemist, occupational health and safety specialist in chemical and microbiological laboratories, management systems auditor (ISO 45001:2018, ISO 14001:2015) and president of the management board of the Polish Training and Consulting Center PCSK Sp. z o.o.
Safety data sheet in 3 seconds - scan and work safely
During this lecture, we will demonstrate how to easily ensure quick and compliant access to safety data sheets in accordance with REACH Regulation 1907/2006, Articles 31 and 35, and CLP Regulation 1272/2008, in daily laboratory work. We will present the Scharlau application, based on QR code scanning, which eliminates the hassle of searching for documentation and streamlines work with hazardous substances. This practical approach truly supports the safety and convenience of laboratory work.


10:30 - 11:00
Apleona Polska Mateusz Kawa
Tomasz Stepaniuk
Full control in the pharmacy. Integrated facility management.

11:00 - 11:15
Pharmalogics Viktoria Babenko
New EU pharmaceutical legislation – what should we expect?
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11:15 - 12:00
apteka.online Oghenekaro Ohimor
Pharmacy Meets Technology: How We're Building a Next-Generation Platform.



12:00 - 12:45
Science Pharma Anna Bieńkowska
Joanna Pawlak
Joanna Popiołkiewicz
Oghenekaro Ohimor — magister farmacji, na co dzień pracujący za pierwszym stołem w aptece ogólnodostępnej. Absolwent Wydziału Farmaceutycznego Uniwersytetu Medycznego w Białymstoku oraz studiów podyplomowych z opieki farmaceutycznej w geriatrii na Uniwersytecie Medycznym w Poznaniu. W zespole apteka.online odpowiada za projektowanie i wdrażanie modułów związanych z usługami farmaceutycznymi oraz współpracę z partnerami B2B. Łączy codzienną praktykę farmaceutyczną z rozwojem cyfrowych narzędzi dla branży — podczas wykładu opowie o tym, jak adaptujemy platformę technologiczną do dynamicznie zmieniającego się świata e-usług farmaceutycznych.
Conference Organizer
Polish Centre for Testing and Certification
Conference room 1
Hall B
IVDR – From Theory to Practice
The event is aimed at IVD manufacturers as well as regulatory and quality specialists, focusing on the practical implementation of IVDR requirements. The program includes topics related to point-of-care testing (POCT) devices – from the regulatory approach to guidance supporting preparation for conformity assessment. The expert program will also be discussed, including the principles of recruitment and cooperation with external experts. A significant part will be dedicated to presenting the role of the notified body in the conformity assessment process, as well as practical aspects of communication within structured dialogue with the manufacturer, supporting an efficient and smooth assessment process.
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13:00
Ewa Domagała – Conference Moderator
Agnieszka Bukowska - Openning Conference
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13:00 - 13:30
Daniel Woliński
In Vitro Diagnostic Medical Devices from the Perspective of a Notified Body
An introductory lecture on the definition and classification of medical devices forin vitro diagnostics and the process of certifying their compliance with Regulation (EU)2017/746
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13:30 - 14:00
dr n. med. Paulina Cembrowska
In vitro diagnostic medical devices used outside the laboratory and their users
Discussion and comparison of the concepts: Near-patient testing (NPT), Point-of-caretesting (POCT), and Self-testing in the context of legal and regulatory requirements, along withpractical implications for in vitro diagnostic medical devices
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14:00 - 14:40
Izabela Czeluśniak
Structured dialogue with a notified body
The presentation will demonstrate how to conduct a structured dialogue with anotified body: principles, scope, process, and examples of topics that can be discussed.
The key differences between a dialogue and a consultation will be explained, andbest practices for preparing questions, documenting findings, and planning actionsfollowing the meeting will be presented.
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14:40 - 15:00
Daniel Woliński
Expert Program of the Medical Office of the Polish Center for Testing and Certification S.A. – a new career path
Discussion and comparison of the concepts: Near-patient testing (NPT), Point- A model of cooperation with the Polish Center for Research andCertification S.A. from the perspective of an external expert involved in thecertification processes of medical devices
Conference Organizer
District Pharmaceutical Chamber in Warsaw
Conference room 1
Hall B
New technologies transforming pharmacy: from algorithms to automation
Pharmacy is at a turning point today. The digitalization of healthcare is accelerating, artificial intelligence and automation are increasingly entering everyday practice, and data is becoming one of the most valuable resources in the system. It is at the intersection of these three areas—technology, information, and patient care—that a new model of pharmacy is taking shape.
The discussion is dedicated to how algorithms, robotics, and data integration are truly transforming the work of pharmacists, the organization of pharmacies, as well as the safety and quality of therapy. We will try to answer not only which technologies will be key, but above all, what challenges, risks, and decisions the entire sector is facing today.
11:00
Opening: Welcome to the participants and the audience
Brief introduction to the topic
Trends and directions of change




Moderator: MSc Pharm. Anita Jeglińska
PharmD Jerzy Żabiński
Konrad Madejczyk, Office of the Patient Ombudsman
Marcin Gawroński, EMEA Regional Innovation Lead at IQVIA and co-owner of Rxbotics Solution Sp. z o.o.
Marian Witkowski, President of the Regional Pharmaceutical Council (District Pharmaceutical Chamber – OIA) in Warsaw Vice-President of the Supreme Pharmaceutical Council (Naczelna Rada Aptekarska) Pharmacist, Pharmaceutical Consultant, Trainer in Pharmaceutical Law
Expert questions
Discussion
Questions from the audience
Summary
patrons of the trade fair and conference
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Speakers' comments
See what else we have prepared
Celebrating Excellence: Medal Awards Ceremony
This event honors the best of the best, highlighting their contributions to the industry’s development and showcasing the most advanced solutions in the following categories:
Trade Fair Premiere: Recognition for exhibitors who introduced innovative products or services at the fair, presenting them to the public for the first time.
Innovation: An award for companies that have presented groundbreaking technologies or solutions with the potential to revolutionize the industry.
Trade Fair Display: A prize awarded for exceptional booth design and aesthetics that stand out for their creativity and attract visitors’ attention.
Trade Fair Product: An award for exhibitors whose product stands out for its quality, functionality, and significance for the industry’s development, earning recognition from both visitors and experts.
The trade fair studio
We invite you to the Trade Fair Studio, where during exclusive interviews with industry experts and outstanding exhibitors, you will learn about the latest trends and innovative solutions. In this inspiring environment, market leaders will share their experiences and visions for the future, providing valuable insights and knowledge. The Trade Fair Studio is also connected with the Medal Award Ceremony, where distinguished exhibitors are honored, adding prestige to the event and highlighting the importance of innovation and excellence in the industry..
Inspiring conversations and new opportunities – the networking zone awaits!
The B2B Networking Zone is an extension of the conference, offering participants a unique opportunity to engage in direct discussions with speakers and other industry experts. In this zone, attendees can exchange insights, ask questions, and establish valuable business connections in a more informal atmosphere.
Join us to deepen your knowledge, continue the inspiring discussions from the conference, and form valuable relationships that can benefit both you and your company!