SYMBIOSIS – a trusted partner in pharmaceutical excellence

SYMBIOSIS has established a long-standing tradition as a specialised service provider for the pharmaceutical and biotechnology industries. Since our founding, our work has been guided by scientific precision, regulatory expertise, and a collaborative partnership approach, earning us the reputation as “the lab that thinks ahead.”

Our fully integrated, end-to-end approach ensures seamless processes and maximum data transparency throughout the entire product lifecycle – from early development to commercial release. This methodology provides the planning certainty required to meet critical milestones efficiently and reliably.

The foundation of our success is our experienced team of long-serving experts. Their deep knowledge of advanced analytical technologies, combined with certified GMP expertise and a GLP-capable quality system, ensures robust data, scientific reliability, and proactive problem-solving. SYMBIOSIS operates in a GLP-capable system and can conduct GLP-certified studies upon client request.

SYMBIOSIS has delivered analytical excellence for almost 40 years across both biopharmaceuticals and classical pharmaceuticals. The company has successfully undergone an FDA inspection and operates in compliance with EMA and COFEPRIS requirements, ensuring regulatory reliability and international compliance.

Integration into the MEX-Group expands our resources and service portfolio, providing scalability while maintaining the personalised support and agility of a specialised provider.

Core competencies at a glance

  • Experienced: Almost 40 years in pharmaceutical analytics
  • Secure: GMP-certified, GLP-capable quality systems
  • Regulatory compliance: FDA- and COFEPRIS-inspected; aligned with EMA
  • Partnership-driven: Dedicated, long-term experts
  • Global: Support for European, Latin American, and international market approvals
  • Modern: State-of-the-art laboratory technology and data-driven processes

Trust a partner for whom scientific rigor and quality ensure your project’s success.

Compliance & Quality

The highest quality is the basis of your success – and our commitment to every analysis we perform.
Through a comprehensive quality assurance system, rigorous quality controls, and proven analytical methods, we deliver results you can rely on.

  • Reliable data that meet international standards
  • Regulatory compliance and security throughout your development and approval processes
  • Efficiency and precision that make your projects predictable and goal-oriented

With our GMP certification, a GLP-capable system, a successful FDA inspection, adherence to EMA and COFEPRIS requirements, and almost  40 years of experience, you benefit from:

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Quality Assurance System

Our quality assurance system ensures that every analysis is conducted transparently, traceably, and reliably – from sample receipt to final report.

By integrating current FDA and EMA requirements, our system remains continuously up to date. Regulatory inspections and client audits regularly confirm full compliance with current GMP standards.

  • Reliable results through clearly defined procedures and documentation
  • Consistent quality through OOS, deviation, and CAPA management
  • Long-term traceability via archiving of all GMP/GLP documentation for 15 years

Inspections and Audits

Regular inspections and audits ensure the consistent adherence to our high-quality standards.
In addition to internal self-inspections, regulatory inspections and client audits are an integral part of our QA system.

This guarantees that you can always rely on the highest level of quality and regulatory assurance.

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