SOP development for cosmetics GMP; Development the program of internal audits; Carrying out internal audits; Choosing outsourcing laboratories in accordance with GMP standard; Confirmation the compliance of cosmetic products with the requirements of TR CU 009; State registration of products for children TR CU 007; Confirmation the compliance of the package with the requirements of TR CU 005; Development of technical specifications for products. Development programs of researches for the confirmation of compliance. Organizing new products researches in accredited laboratory. Composing PIF for products that are exported to Europe. Obtaining gtin13, ITF14. Checking the labeling for compliance with the established requirements.

Preparing of the laboratory for accreditation in accordance with GOST ISO / IEC 17025-2019: development of procedures and policies in accordance with this standard, modification of existing procedures and quality guidelines; Check quality control protocols of drugs (a part of batch file); Сonducting self-inspections; QMS laboratory effectiveness assessment;. Development of measures to improve and increase the effectiveness laboratory QMS; Taking part in investigations and development of CAPA, monitoring its performance and efficiency.

Organisation of laboratorian activity according to ISO 17025; Obtaining declarations of conformity TR CU 009; Development of technical specifications for new products; Development industrial and laboratorian SOP and instructions in accordance with GMP and ISO 9001 standards; Development CAPA, monitoring its performance and efficiency; Management staff of the analytical laboratory; Development of External training plans for staff ; Supplying of laboratory with reagents and standard samples; Approval cosmetic products labeling; Metrological maintenance of laboratory equipment Preparing product files for state registration of (cosmetics) and medical devices; Working with outsourcing organizations State registration of food supplements( in Belarussian Ministry of healthcare department)-additional job

State registration of food supplements; State registration of veterinary medicines through Belarus; Development of technical specifications for veterinary medicines; Confirmation of products compliance with the requirements of TR CU 021, TR CU 022, TR CU 005, TR CU 017 for importers and manufacturers of Belarus and Russia (Declararions of conformity ); Development and registration of Technical specifications for cosmetics, food supplements etc. Development ISO 9001 procedures for clients for further certification. Development laboratory center project for the for the researches of food products for confirmation of compliance with the requirements of TR CU 021, TR CU 033, TR CU 024 and ND (selection the equipment, and counting of total price, selection of methods of control, layout of premises); State registration of products within the CU ( obtaining CSR) for Russian companies through Minsk.

Development schemes of chemical and microbiological control; Supplying the Laboratory with necessary equipment, materials and reagents; Preparing laboratory for accreditation according to ISO 17025 standards; Development specifications for raw materials and ready made products; Development of technical specifications for new products; Obtaining declarations of conformity TR CU; Obtaining Kosher certificate; Development information for customers (ingredients, nutrition facts etc) for Russian Federation, Germany, Lithuania, Latvia, Belarus, USA, Canada, China, South America.

Development GMP documentation in accordance with WHO and ICH guidelines and local standards. Implementation and maintenance of the GMP; Conducting self-inspections; Development of CAPA programs, monitoring performance and efficiency; Carrying out the procedure of registration for food supplements and veterinary medicines. Development of technical specifications for new products.

Design and development laboratory from 0; Supplying the industrial laboratory with necessary equipment, materials and reagents; Preparing laboratory for accreditation according to ISO 17025 standards; Chemical control of beer (finished product: spirit content and content of dry substances in initial wort, actual extract, acidity, color) and preparation of Quality certificates; Chemical control of wort; Chemical control of raw materials; Carrying out the procedure confirmation of compliance of beer and raw materials with requirements CU TR; Development of technical specifications for new products.

Incoming control of API, raw materials and packaging; Calculating the quantity of API, raw materials and packaging necessary for the technological process; Technological parameters control ; Chemical checking of finished veterinary medicines and dietary supplements (active substance identification and content such as chlorhexidine bigluconate, Vitamine A, quaternary ammonium compounds, etc.) using high perfomance liquid chromatography, spectrophotometry, etc.; Development and validation of analytical methodics dietary supplements for human and veterinary medicines analysis using USP, Eur.Ph. methods of analysis; Development of technical specifications for veterinary medicines and food supplements for human; Development of technical conditions for veterinary medicines; Carrying out the procedure of certification for dietary supplements and veterinary.

Development GMP documentation in accordance with WHO and ICH guidelines and local standards. Implementation and maintenance of the GMP; Conducting internal audits and inspections and Reporting; Development of corrective action programs, monitoring performance and efficiency Development of technical specifications for the dietary supplements; Development of technical documentation; Development of analytical methods for drugs and food supplements; Carrying out the procedure of certification for finished products.

Development of technical specifications for the cosmetics; Development of technical documentation; Development of quality control methods for cosmetics; Carrying out the procedure of certification cosmetics and perfumery; Development of ISO 9001 documentation, implementation of QMS, certification and maintenance; Сonducting self-inspections; QMS effectiveness assessment;. Development of measures to improve and increase the effectiveness laboratory QMS; Taking part in investigations and development of CAPA, monitoring its performance and efficiency.

Transfer of the technology of hydrogel wound dressings production and adjustment technological process; Incoming control of raw materials and packaging; Calculating the quantity of reagents for the technological process of hydrogel wound dressings production; Control of technological parameters hydrogel wound dressings production; Maintenance the routine process documentation and records. Making progress more fast and cheap.

Control of sanitary conditions of production; Microbiological control of finished dairy products (identification and defining content of lactic acid bacteria in products, defining CFU, coliforms, pathogenic microorganism Salmonella, Staphylococcus); Microbiological control of raw materials and products during technological process; Carrying out the accreditation of microbiological laboratory. .