Czech company, founded in 1991.

Since 2000, the representative office in Moscow in the Russian Federation.

Lab & Pharma company is a team of experienced specialists, more than half of whom have been working in the company for more than 10 years. During Lab&Pharma existence, we have worked on more than 140 projects that have been successfully completed, put into operation and operate reliably.

Lab&Pharma is engaged in designing new and reconstructed pharmaceutical and biotechnological plants and laboratories, supplying engineering systems, clean rooms and functional technological units including their commissioning.

When working, Lab&Pharma staff follows, among others, the requirements of GMP, ISO, ISPE, FDA, PDA, WHO, hygiene and fire regulations, building and technical regulations valid in the countries of their work, and environmental regulations.

Standardly, Lab&Pharma works in Czech, Russian and English for the customers in the Czech Republic, Slovakia, Russia, Ukraine, Belarus, Uzbekistan and other countries.

20 specialists of Lab&Pharma hold personal licences (Czech ones) for designing, assembly management and start-up in different special disciplines (civil engineering, stress analysis and steel structures, heating engineering, air conditioning, sanitary engineering, electrical, process equipment for factories and special plants).

Since 2010, Lab&Pharma  has been a member of SRO „Mezhdunarodnoe obedinenie projektirovshchikov“ (Internationa Designers Union) and SRO „Mezhdunarodny alians stroiteley“ (International Constructors Alliance) and holds the competency certificate for designing and the competency certificate for construction-and-assembly (installation) and start-up works in the Russian Federation.

Lab&Pharma offers comprehensive design preparation services, design implementation and subsequent technical support.

For the existing facilities – we offer

• Analysis of possible problems, proposal for solution and problem removal.
• Consultation in the field of GMP, technological equipment, clean rooms, monitoring of critical parameters and other areas of pharmaceutical production.
• Development of the existing facility reconstruction design:
  • Conceptual study.
  • Design documentation for building permit.
  • Design documentation for construction.
  • As-built documentation.
  • Designer´s on-site supervision during construction.
• Development of user requirement specifications – URS – for newly integrated technological equipment.
• Technical support in selection of new technological equipment.
• Technical support during FAT/SAT of the new technological equipment.
• Integration of new technological equipment into the existing plant (facility) and its connection to the media.
• Modification and extension of the existing systems, deliveries and assembly/installation:
  • Clean rooms and HVAC.
  • Process media – utilities (water for injection, purified water, pure steam, compressed air, technical gases).
  • Solution preparation systems.
  • CIP, SIP systems.
  • Identification of causes of problems in the existing systems, inspection of stainless systems of technological media, product pipelines, etc. and their possible repair or reconstruction.
  • Critical parameter monitoring system (particle, air flow speed, pressure, temperature, humidity).
  • Engineering systems (HVAC, cooling, heating, steam, wiring, automated control, water pipeline, drains).
• Sub-deliveries of specialized parts of the systems for other suppliers.
• Adjustment (balancing) of the existing HVAC and engineering systems, defectoscopy of HEPA filters.

• Preparation of commissioning testing documents and performing the tests.

• During all the phases, we work closely with the customer´s specialists.
• Technical support for maintenance of the systems delivered by Lab&Pharma for their whole lifetime, or their regular contractual servicing.

For the newly constructed facilities – we offer

• Consultation in the field of GMP, technological equipment, clean rooms, monitoring of critical parameters and other areas of pharmaceutical production.
• Development of the new facility design:
  • Feasibility study.
  • Conceptual study.
  • Basic design.
  • Design documentation for building permit.
  • Design documentation for construction.
  • As-built documentation.
  • Designer´s on-site supervision during construction.
• Development of user requirement specifications – URS – for technological equipment.
• Technical support in selection of technological equipment.
• Technical support during FAT/SAT of technological equipment.
• Integration of technological equipment into the clean room and its connection to the media.
• Delivery and assembly/installation:
  • Process media – utilities (water for injection, purified water, pure steam, compressed air, technical
    gases).
  • Delivery of specialized manufacturing equipment.
  • Solution preparation systems.
  • CIP, SIP systems.
  • Design and delivery of clean room equipment.
  • Critical parameter monitoring system (particle, air flow speed, pressure, temperature, humidity).
  • Engineering systems (HVAC, cooling, heating, steam, wiring, automated control, water pipeline, drains).
• Sub-deliveries of specialized parts of the systems for other suppliers.
• Commissioning of HVAC and engineering systems, testing and adjustment (balancing) of the systems, defectoscopy of HEPA filters incl. preparation of operating and maintenance manuals and training of operating staff.
• Preparation of commissioning testing documents and performing the tests.
• During all the phases, we work closely with the customer´s specialists.
• Technical support for maintenance of the systems delivered by Lab&Pharma for their whole lifetime, or their regular contractual servising.