Labochem
Commercial supplier and service provider for pharmaceutical, food, cosmetic and chemical industries. Offers bioequivalence study support in collaboration with external laboratories, bioanalytical method development and pharmacokinetic analysis; sources APIs and packaging materials with supporting quality documentation; supplies, integrates and commissions processing and packaging machinery and turnkey GMP cleanrooms; provides regulated importation and qualified person (QP) release services and analytical impurity testing supported by a GMP certificate.
Industries
Nr. of Employees
small (1-50)
Products
Packaging materials for food, pharma and cosmetics
Primary and secondary packaging materials including ampoules, vials, aluminium aerosol cans, tubes, laminate and flexible films, printed or unprinted options suitable for GMP environments.
Processing and packaging machinery for food, chemical and pharmaceutical industries
Machines and complete lines for product processing and packaging including mixers, granulators, tablet presses, fillers, capping and induction sealers, blistering, cartoning, vertical FFS and end-of-line equipment with inspection integrations.
Distribution of active pharmaceutical ingredients (APIs)
Sourcing and distribution of APIs with supporting quality documentation and supplier audit records for local pharmaceutical manufacturing.
Packaging materials for food, pharma and cosmetics
Primary and secondary packaging materials including ampoules, vials, aluminium aerosol cans, tubes, laminate and flexible films, printed or unprinted options suitable for GMP environments.
Processing and packaging machinery for food, chemical and pharmaceutical industries
Machines and complete lines for product processing and packaging including mixers, granulators, tablet presses, fillers, capping and induction sealers, blistering, cartoning, vertical FFS and end-of-line equipment with inspection integrations.
Distribution of active pharmaceutical ingredients (APIs)
Sourcing and distribution of APIs with supporting quality documentation and supplier audit records for local pharmaceutical manufacturing.
Services
End-to-end bioequivalence study services including protocol design, clinical phase coordination, bioanalytical method development, PK analysis, statistical programming and dossier writing.
Regulatory handling of importation and qualified person release for non-sterile semi-finished products sourced outside the EU, including license submission support.
Study, design and construction of GMP cleanrooms and turnkey pharmaceutical factories, including process certification and utilities design.
Installation and commissioning of supplied machinery and on-site training for customer personnel on operation and maintenance.
Supply, specification and integration of processing, filling, packaging and end-of-line inspection equipment for food, chemical and pharmaceutical production.
Supply and installation of personnel hygiene stations, hand and shoe sanitizers, equipment washers and sanitization lines for production environments.
End-to-end bioequivalence study services including protocol design, clinical phase coordination, bioanalytical method development, PK analysis, statistical programming and dossier writing.
Regulatory handling of importation and qualified person release for non-sterile semi-finished products sourced outside the EU, including license submission support.
Study, design and construction of GMP cleanrooms and turnkey pharmaceutical factories, including process certification and utilities design.
Installation and commissioning of supplied machinery and on-site training for customer personnel on operation and maintenance.
Supply, specification and integration of processing, filling, packaging and end-of-line inspection equipment for food, chemical and pharmaceutical production.
Supply and installation of personnel hygiene stations, hand and shoe sanitizers, equipment washers and sanitization lines for production environments.
Expertise Areas
- Bioequivalence study management
- Bioanalytical method development and validation
- Pharmacokinetic analysis and statistical programming
- Regulatory dossier preparation and QP release for imports
Key Technologies
- High-shear mixing
- Fluid bed granulation and drying
- Tablet compression and capsule filling
- Liquid filling and capping systems
News & Updates
Company participation at the CPhI exhibition in Frankfurt to discuss product development, finished products supply and APIs; event held October 28-30, 2025.
Installation and commissioning of cartoner, X-ray inspection, metal detector and grinding mill for an agricultural cooperative; included personnel training by technical department.
Hosted/participated in a scientific symposium on pharmaceutical and biopharmaceutical development covering bioequivalence studies, peptide characterization, preclinical and clinical development and GMP analytical capabilities; held September 18, 2025.
Company participation at the CPhI exhibition in Frankfurt to discuss product development, finished products supply and APIs; event held October 28-30, 2025.
Installation and commissioning of cartoner, X-ray inspection, metal detector and grinding mill for an agricultural cooperative; included personnel training by technical department.
Hosted/participated in a scientific symposium on pharmaceutical and biopharmaceutical development covering bioequivalence studies, peptide characterization, preclinical and clinical development and GMP analytical capabilities; held September 18, 2025.