Basic, Advanced & Custom setups for different tasks with nothing redundant for cost optimization.
Simple architecture and sound technological solutions, main components from industry leaders.
Service center in Baltics, full-time support for European customers, 24h for engineers to arrive.
We follow and adhere to the guidelines as set forth for cGMP, GAMP and FDA where requested.
BRS Biotech is an international company with headquarters in Baltics.
We make affordable and reliable equipment for biotech, pharma, food industries. We use simple architecture and sound technological solutions with main components supplied by industry leaders. We strive for easy and trouble-free setup, maintenance and operation.
MORE ABOUT OUR COMPANY We manage production facilities ready for large-scale projects with vessels volumes up to 60000 l.
R&D team consists of 4 lead engineers, 4 technical drawing specialists, 1 QA manager, 3 technical designers, 2 quality inspectors.
Automatic welding (ESAB – 1, APUS – 1), Semi-auto welding (ESAB – 1, LINCOLN – 1), Welding heads (ESAB, LINCOLN, SELCO, Kemppi – 22 total), ORBITALUM pipe cutting – 4, Gravitational bandsaw – 2, Radial drilling machine – 2, Metal lathe – 2, Plasma cutter – 1, Flanging machine – 1, Vessel rotators – 2.
Please feel free to contact Kate 9.00-17.00 CET.
You can send us inquiry by filling
DETAILED QUESTIONNAIRE
Industrial Fermentors and Bioreactors The BRS portfolio of single-use solutions for upstream processes includes rocker and stirred tank bioreactors, single-use mixers and all necessary accessories.
Clean-In-Place Systems BRS cleaning and sterilization systems are designed for effective sanitization of equipment and instruments.
Warning: Undefined array key 0 in
/var/www/u1333635/data/www/brsbiotech.com/wp-content/plugins/Ultimate_VC_Addons/modules/ultimate_functions.php on line
252
Conceptual Design
Basic GMP Risk Analysis / Validation Master Plan + User Requirements Specification
Basic Design
Detailed GMP Risk Analysis + Design Qualification
Equipment Manufacturing
Factory Acceptance Test (Equipment Manufacturers Site)
Delivery & Installation
Installation Qualification
Start-Up
Operational Qualification
Commissioning
Site Acceptance Test (Clients Site)
Process Optimization
Process Validation / Cleaning Validation
Routine Production
Regular Revalidation
GMP compliant design and documentation
Design and manufacturing is carried out in accordance with FDA and GMP standards.
Full documentation includes: FAT, IQ, OQ, DQ, Manual and maintance, Сad layout drawing, Main parts/spare parts list, SAT, Factory’s certificate, PLC software operation copy.
We can also implement a full range of validation services:
CLV – Cleaning Validation
DQ – Design Qualification
FAT – Factory Acceptance Test (Equipment Manufacturers Site)
GAMP – Good Automated Manufacturing Practice
IQ – Installation Qualification
OQ – Operational Qualification
PQ – Performance Qualification
PV – Process Validation
RA – GMP Risk Analysis
SAT – Site Acceptance Test (Clients Site)
URS – User Requirements Specification
VMP – Validation Master Plan
We finished the installation of a laboratory bioreactor 10 L with an optical density sensor.
Read more We successfully installed a glass bioreactor with total volume 3L.
Read more For our customers, this bioreactor was an ideal solution for the cultivation of aquatic organisms, namely cells and tissues of micro- and macroalgae.
Read more CENTRIFUGE INSTALLATION VIDEO