SIX8 supports pharmaceutical and life sciences organizations across testing, product development, quality assurance, documentation, and regulatory requirements through coordinated technical capabilities and qualified laboratory partners.
PHARMA TESTING | PHARMA R&D | QA & REGULATORY
5+
Specialized technical and laboratory capabilities across key requirements
10+
Analytical, microbiological and stability testing support
1
One point of contact across testing, R&D and quality requirements
360°
From analytical testing and development to quality documentation
INTRODUCING SIX8 LIFE SCIENCE
From analytical testing and stability studies to R&D support, quality documentation, and regulatory requirements, SIX8 helps pharmaceutical organizations navigate critical technical and quality activities with greater clarity and coordination.
We coordinate with qualified laboratories and technical service partners to support specific testing, development, quality, and documentation requirements based on each engagement.
Our approach is built around scientific rigor, quality, precision, and reliable execution.
SERVICES
01 — Pharma Testing
We coordinate analytical, stability, and microbiological testing through qualified laboratories to support pharmaceutical product and quality requirements.
Services include:
02 — Pharma R&D
We support pharmaceutical R&D activities through analytical, formulation, technical documentation, stability, and development coordination.
Services include:
03 — QA & Regulatory
We support pharmaceutical organizations with quality systems, documentation, validation activities, audit preparation, and regulatory dossier requirements.
Services include:
Our capabilities are designed to support key technical requirements across pharmaceutical development and quality management.
Testing support across pharmaceutical raw materials, finished products, water, microbiology, impurities, assay, and dissolution requirements.
Coordination of stability programs to evaluate product quality and performance over defined conditions and periods.
Support for analytical method development and coordination of method validation activities.
Support for formulation, pre-formulation, excipient selection, technical research, and product development documentation.
Support for SOPs, specifications, batch documentation, COA review, vendor qualification, audits, CAPA, and validation documentation.
Support for organizing and preparing technical and regulatory documentation relevant to pharmaceutical requirements.
WHO WE SUPPORT
Our services are designed to support organizations across the pharmaceutical and life sciences landscape, including:
WHAT WE DO
SIX8 supports pharmaceutical and life sciences organizations with specialized capabilities across testing, R&D, quality, and regulatory requirements.
We coordinate with qualified laboratories and technical partners to support analytical testing, stability studies, product development, technical documentation, quality activities, and regulatory requirements—helping clients move from technical requirements to reliable execution.
Whether you need analytical testing, stability support, technical development assistance, quality documentation, or regulatory support, talk to SIX8 about your requirement.
