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Sercotech – Fertigung

Turn-key projects, engineering and EU-GMP compliance for the pharmaceutical, cosmetic and food industries

Sercotech Logo

SERCOTECH SAGL

Via Valdani 2, 6830 Chiasso, SwitzerlandNew on Amplifa

SAGLLegal form
Chiasso, SwitzerlandLocation
Pharma, Cosmetics, Food & BeverageIndustry focus

About Sercotech

SERCOTECH SAGL, based in Chiasso, Switzerland, is a service company for integrated turn-key project execution in the health sector. Its service portfolio for new facilities includes feasibility studies, site master planning, conceptual design, engineering including laboratory design, technology transfer, procurement of machinery and equipment, construction of production areas, installation and commissioning, as well as qualification and validation (CQV) according to a VMP for obtaining GMP approval. For existing operations, the company offers EU-GMP and CMP compliance services, including implementation and upgrading of GMP systems, audits and inspections for ISO and CMP conformity, QM systems according to DIN EN ISO 13485 and 9001, risk-based qualification, validation, GMP training and regulatory affairs. In addition, Sercotech supplies raw materials for chemical synthesis such as building blocks, chiral auxiliaries, protective groups, reagents and solvents, as well as pharmaceutical, laboratory and medical technology consumables. The company also supplies and maintains machinery and equipment, including liquid processing and packaging solutions for parenteral products, solutions, suspensions and syrups. Its activities focus on the pharmaceutical, cosmetic and food & beverage industries.

Site
Chiasso
Processes
Design and engineering services, Facility concept and planning – feasibility studies, Site master planning, Conceptual design, Laboratory design, engineering and construction, EU GMP compliance services (GMP system implementation, audits, qualification, validation), Commissioning, qualification, validation and training (CQV), Cleanroom operation and technology
Materials
Building Blocks, Chiral Auxiliaries, Protective Groups, Reagents, Solvents, Excipient/active pharmaceutical ingredient (API), Excipient / API
Industries
Pharmaceutical industry, Cosmetics, Food & Beverage, Life Sciences
  1. 01

    Feasibility study

  2. 02

    Site master planning

  3. 03

    Conceptual design

  4. 04

    Engineering (incl. laboratory design)

  5. 05

    Technology transfer

  6. 06

    Procurement of machinery and equipment

  7. 07

    Construction of production areas

  8. 08

    Installation and commissioning

  9. 09

    Qualification and validation (CQV)

  10. 10

    Training and regulatory affairs

  11. 11

    Supply of raw materials and consumables

Raw Materials & Product Range

BB

Building Blocks

Basic building blocks for chemical synthesis in the pharmaceutical industry.

CA

Chiral Auxiliaries

Chiral auxiliaries for chemical synthesis in pharmaceutical production.

PG

Protective Groups

Protective group reagents for chemical synthesis in the pharmaceutical industry.

RE

Reagents

Reagents for pharmaceutical production and laboratory applications.

SOL

Solvents

Solvents for chemical synthesis in the pharmaceutical industry.

API

Excipient / API

Excipients and active ingredients in the context of GMP compliance services.

Location

Standort Chiasso

Chiasso

CH

Headquarters/Office

Inside the production

Pharmaceutical production facility
Pharmaceutical production facility
Installation of an industrial plant
Installation of an industrial plant
Machinery for pharmaceutical liquid processing
Machinery for pharmaceutical liquid processing
Systems and equipment for pharmaceutical production
Systems and equipment for pharmaceutical production
Process engineering equipment
Process engineering equipment
Raw materials for the pharmaceutical industry
Raw materials for the pharmaceutical industry
Pharmaceutical and laboratory consumables
Pharmaceutical and laboratory consumables
Cosmetics production
Cosmetics production
Cosmetics laboratory
Cosmetics laboratory

Industries

Pharmaceutical industryCosmeticsFood & BeverageLife Sciences

Processes & technical limits

ProcessesToleranceMax. partWeightLot sizeMaterials
Engineering–––––
Design and engineering servicesEngineering–––––
Facility concept and planning – feasibility studiesEngineering–––––
Site master planningEngineering–––––
Conceptual designEngineering–––––
Laboratory design, engineering and constructionEngineering–––––
EU GMP compliance services (GMP system implementation, audits, qualification, validation)Testing–––––
Commissioning, qualification, validation and training (CQV)Testing–––––
Cleanroom operation and technologyEngineering–––––
Pharmaceutical aseptic manufacturingEngineering–––––
Process technology and pharmaceutical packagingAssembly–––––
Engineering–––––
Supply of raw materials (building blocks, chiral auxiliaries, protective groups, reagents, solvents)Other–––––
Supply of pharmaceutical, laboratory and medical consumablesOther–––––
Machinery and equipment procurement incl. maintenance and serviceEngineering–––––
Training (personalized, subject-specific)Engineering–––––
Regulatory affairsEngineering–––––
Supply chain managementEngineering–––––

Additional services

Turn-key project executionFeasibility studiesConceptual designSite master planningEngineeringLaboratory design, engineering and constructionTechnology transferProcurement of machinery and equipmentConstruction of production areas, installation and commissioningQualification and validation (CQV, according to VMP for GMP approval)EU GMP compliance servicesStaff trainingRegulatory affairsSupply chain managementSupply of consumables (pharma, laboratory, medical technology)Supply of machinery and equipment (incl. liquid processing and packaging)Maintenance and service for equipment
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