- Methods Development
- Methods Transfer
- Methods Optimization
- Test Specifications
- Environmental Monitoring
- Bioburden Control
- Investigations / CAPAs
- SOPs development and training in Compliance with USP, EP, JP and FDA Guidelines
- Methods Transfer and Validation
- Sanitizing Agents Studies
- Recovery Studies
- Chemical Analysis (Bench Support)
- Laboratory Equipment Qualification
- Microbiology Training Modules
- Chemical Qualitative/Quantitative Analysis of Raw Materials, Finished Goods and Stability
- Empower, Millennium Systems
- CVS
- Project Manager
- IOPQ
- On-Site Trainings
- Custom Programming (Tool kit)
- Custom Fields
- Laboratory Informatics Validation
- High Performance Liquid Chromatographs (HPLC)
- Gas Chromatographs
- Microplate Readers
- UV / Visible Spectrophotometers
- Total Organic Carbon (TOC)
- Near IR
- Data and Acquisition Systems
- Quality Control Testing
- Microbiology Services (Scienzalabs)

Pharmaceutical, Biotechnology, Medical Device, Bulk Manufacturing Industries (Finished Product, Packaging, Stability, API, Raw Materials and Food Industry.):
- Microbial Limits Testing
- USP Organisms
- Microbial ID
- Sterility Testing
- LAL Testing
- Anti-microbial Effectiveness Test
- Media Preparation
- Environmental Testing and Monitoring
- Particles Matter Identification
- Water Testing
- Cleaning Validation Testing
- Bioburden Analysis
- Swab Analysis
Food Industry:
- Disinfectant Validation
- Sanitization
- Environmental Monitoring
- Microbial Testing and Identification
Others:
- Stability Storage
- Stability Protocol Development
- Compress Air Sampling and Testing
- Disinfectant Validation
- Sanitization
- Media Preparation
- Methods Verification & Revision
- Methods Development
- Methods Validation
- On Site Pick Up