MEET US
@ ACHEMA 2024
Frankfurt | 10-14 June | Stand E75, Hall 9
Join us at Achema 2024 to connect with our experts and explore how Elomatic can assist you in creating controlled environments with precision where every step is tailored to your production needs.
We are excited to meet you in Frankfurt Am Main, Germany at our stand E75 in Hall 9.
This year, Elomatic’s theme is “Controlled Environments Created with Precision – Every Step Tailored to Production Needs,” we’re showcasing our expertise in pharmaceutical and medical device production suites. With years of experience and extensive know-how, we specialize in designing, constructing, and qualifying new facilities and production lines. Our collaborative approach involves architects, engineers, operators, and equipment suppliers to ensure your cleanrooms are optimized for efficient production.
In this year’s Achema we’re excited to present our collaborative solutions alongside our subsidiary Naya Life Sciences – a global provider of cleanroom bioprocess technology.
With our collective experience and innovative approaches, we’re here to assist you in designing, constructing, and qualifying cleanroom facilities that meet the highest standards of quality and efficiency.
Join us at Achema to explore how Elomatic and Naya can elevate your production capabilities with tailored cleanroom solutions.
Naya
Naya specializes in delivering complete cleanroom environments for a variety of life science industries, offering solutions ranging from laboratories to manufacturing process platforms and precision medicine applications.
Top Engineer
Energy efficiency in cleanrooms – Dangers of overdesign or under-design
Text: Gligor Mukaetov, Goran Serafimov, Zarko Kostovski
Since the global energy crisis hit, companies in pharmaceutical manufacturing started improving their energy efficiency to contribute to the economy as well as to their budget. Heating, ventilation, and air conditioning (HVAC) systems are typically the biggest energy consumers in pharmaceutical facilities, and design is the best stage at which to influence them.
Join the Congress
“Verification of controlled environments”
A cleanroom should be designed and delivered according to the requirements of the production process and operators. Based on the developed contamination control strategy, the layout and functions of the cleanrooms are defined. The presentation will describe the workflow, roles & responsibilities, and tasks needed from starting the concept design to the final verification of the complete manufacturing suite. Practical ways of performing risk-based and paperless verification are discussed and examples from current projects are presented. The verification of controlled environment should be taken into account in every phase of the delivery.
Mona Åkerholm, Senior Vice President, Pharma at Elomatic
6/13/2024, 10:00 AM – 10:30 AM
Zeta Pharma Innovation Stage – 4.1
Meet the Team
Mona Åkerholm
I have a vast experience in completing investment projects, from conceptual design and investment decisions, through definition and execution to managing commissioning, qualification and handover. By working in international projects all over the world as a project manager, I have gained experience with communicating and motivating teams and experts from several cultures. For a project manager it is important to finalize all assignments within agreed scope and time schedule and also satisfy the customer and project team.
My expert field is process and facility design for biotechnological and pharmaceutical facilities, from facilities requiring special containment to bulk production of common pharmaceuticals and bio-based chemicals. I have also trained companies and organizations in procurement of equipment, validation and documentation and cleanroom design.
My positive attitude towards new challenges and situations gives energy to develop and finalize new products and facilities. In my current position as Senior Vice president for Pharma BU at Elomatic, I’m developing my international network and Elomatic’s offerings for our target customers.
Riikka Peltola has a long experience working in pharmaceutical industry and in GMP environment. Since her graduation in Biotechnology, her career has progressed through various stages in research, product development, commercial production and business operations in pharmaceutical industry. She also holds MBA degree and is experienced in customer relationship management having a strong background working with both big pharma customers and start-ups. She is at your disposal for the discussions of your investment project needs when designing, constructing and qualifying new facilities and production lines – in all investment phases; from concept to execution. Riikka desires to ensure that your needs are heard and encompassed over the course of the project.
Semih Geyik brings over a decade of industry expertise to the table, specializing in operations and project management within the pharmaceutical sector. With a comprehensive background spanning more than five years in factory management, particularly with cleanroom equipment and components, Semih excels in leading teams through project lifecycles from design to execution while upholding exceptional quality standards. Renowned for his strategic acumen and problem-solving prowess, Semih boasts a proven track record of delivering cleanroom projects that exceed customer expectations.
Gligor Mukaetov is a distinguished expert in pharmaceutical engineering, with over 10 years of industry experience. His extensive knowledge covers various facets of pharmaceutical engineering, including HVAC design, equipment selection, regulatory compliance, and quality assurance. Gligor is acclaimed for his outstanding problem-solving skills, strategic thinking, and implementation of innovative solutions that drive efficiency and innovation in cleanroom design.
Seray Merve Demirli, equipped with a background in Civil Engineering and an MBA degree, brings a unique blend of technical expertise and business acumen to the cleanroom industry. Starting as a cleanroom designer, Seray swiftly ascended through the ranks, holding key roles such as Design Manager and Operations Lead at a specialized cleanroom production facility. Fueled by a passion for innovation and an unwavering commitment to excellence, she consistently delivers exceptional results, ensuring client satisfaction and spearheading business expansion alongside her team. With a focus on providing holistic solutions for contamination control, Seray’s dedication shines through in every project she undertakes.
Arash Zamani, a dedicated project manager with a background in Biology and Chemical Engineering, brings a wealth of experience from the biotechnology industry. Having held various leadership positions, including Executive Director and Chief Operating Officer, Arash is adept at Bioprocess Design and has a proven track record of successfully managing projects in the pharmaceutical sector. Passionate about fostering innovation and excellence, Arash currently serves as the Business Development Manager, playing a pivotal role in driving growth and cultivating strategic partnerships for the organization.
Miroslav Tonovski, Chief Executive Officer of NAYA Life Sciences, brings a background in Mechanical Engineering and boasts over 25 years of experience in maintaining clean environments across industries where contamination control is paramount. With an exceptional passion for innovation, extensive expertise, and strong leadership acumen, he spearheads the growth and excellence of NAYA Life Sciences. Notably, he authored Chapter 7 of “Cleanroom Management in Pharmaceuticals and Healthcare,” edited by Dr. Tim Sandle, highlighting his in-dept knowledge in the field. As an active member of the International Confederation of Contamination Control Societies, he remains dedicated to advancing global standards in contamination control.
Book a Meeting @ACHEMA 2024
Insights
Pharma
We offer strong expertise in pharmaceutical and medical device production suites.
We help you in designing, constructing, and qualifying new facilities and production lines. Our services encompass all investment phases, from creating a concept to delivering the final report.
EloTalk season 2
In the EloTalk episodes, we delve into the role of technology in building a responsible and sustainable future. Yes, the connection between these elements is likely understood by everyone, even though the transition from words to actions isn’t always clear. In the second season’s episodes, we intertwine technology and humanism, the sustainability of the planet and human well-being, engineering sciences and emotions.
Energy efficiency in cleanrooms – Dangers of overdesign or under-design
Since the global energy crisis hit, companies in pharmaceutical manufacturing started improving their energy efficiency to contribute to the economy as well as to their budget. Heating, ventilation, and air conditioning (HVAC) systems are typically the biggest energy consumers in pharmaceutical facilities, and design is the best stage at which to influence them.
Elomatic has been chosen to design the clean rooms and implement the space for the new Biovian Oy manufacturing facility in Turku, Finland.
The new facility will cover an area of 6,400 sqm and house cutting-edge equipment and advanced technologies to provide vital therapies to patients suffering from today’s untreatable diseases. It will also feature dedicated Class A to D cleanroom areas for bulk drug substances as well as final drug product manufacture.