Our Services
Comprehensive laboratory solutions for pharmaceutical development
Comprehensive Laboratory Services
At Reddy Anna, we offer a wide range of laboratory services designed to support pharmaceutical companies throughout the drug development lifecycle. Our state-of-the-art facilities and experienced team ensure that you receive accurate, reliable, and timely results.
Whether you need analytical testing, formulation development, stability studies, or regulatory support, our team is equipped with the knowledge and technology to meet your specific requirements. We pride ourselves on providing customized solutions that address the unique challenges of each project.
Explore our services below and discover how Reddy Anna can support your pharmaceutical development needs.
Analytical Testing
Our comprehensive analytical testing services provide accurate and reliable data to support your pharmaceutical development and quality control needs. Using state-of-the-art equipment and validated methods, we deliver precise results that meet regulatory requirements.
Our Analytical Testing Services Include:
- Method development and validation
- Raw material testing and characterization
- Impurity profiling and identification
- Release testing of finished products
- Dissolution testing
- Particle size analysis
- Chromatographic analysis (HPLC, GC, UPLC)
- Spectroscopic analysis (UV, IR, NMR)
- Elemental analysis
- Microbial testing
Formulation Development
Our formulation development services help you create stable, effective, and manufacturable pharmaceutical products. We combine scientific expertise with practical knowledge to develop formulations that meet your target product profile.
Our Formulation Development Services Include:
- Pre-formulation studies
- Excipient compatibility studies
- Prototype formulation development
- Process optimization
- Scale-up support
- Formulation of various dosage forms:
- Oral solid dosage forms (tablets, capsules)
- Semi-solid formulations (creams, ointments, gels)
- Liquid formulations (solutions, suspensions)
- Modified release formulations
- Quality by Design (QbD) implementation
- Technology transfer support
Stability Studies
Our stability studies provide crucial information about how your pharmaceutical products perform over time under various environmental conditions. We conduct comprehensive stability testing to support product development, registration, and shelf-life determination.
Our Stability Study Services Include:
- ICH-compliant stability studies
- Accelerated stability testing
- Long-term stability studies
- Photostability studies
- Forced degradation studies
- Temperature cycling studies
- In-use stability testing
- Stability-indicating method development
- Stability data analysis and reporting
- Shelf-life determination
Bioequivalence/Clinical Support
Our bioequivalence and clinical support services help you generate the data needed for regulatory submissions and product approvals. We provide comprehensive analytical support for bioequivalence studies and clinical trials.
Our Bioequivalence/Clinical Support Services Include:
- Bioanalytical method development and validation
- Sample analysis for bioequivalence studies
- Pharmacokinetic (PK) sample analysis
- In vitro-in vivo correlation (IVIVC) studies
- Clinical trial material preparation
- Analytical support for clinical trials
- Biomarker analysis
- Data interpretation and reporting
Note: Reddy Anna provides analytical and laboratory support for bioequivalence studies and clinical trials but does not conduct clinical trials on human subjects.
Request Bioequivalence Support
Contract Research
Our contract research services provide flexible and customized solutions for your pharmaceutical research needs. We offer expertise, facilities, and resources to help you advance your research projects efficiently and cost-effectively.
Our Contract Research Services Include:
- Custom synthesis of reference compounds and impurities
- Process development and optimization
- Analytical method development
- Formulation screening and optimization
- Compatibility studies
- Degradation pathway identification
- Crystallization studies
- Salt selection and polymorph screening
- Collaborative research projects
Regulatory Documentation Support
Our regulatory documentation support services help you navigate the complex regulatory landscape and prepare comprehensive documentation for regulatory submissions. We ensure that your documentation meets the requirements of regulatory authorities in India and around the world.
Our Regulatory Documentation Support Services Include:
- Common Technical Document (CTD) preparation
- Quality Overall Summary (QOS) preparation
- Method validation reports
- Stability data compilation and analysis
- Analytical method transfer protocols and reports
- Gap analysis for regulatory submissions
- Response to regulatory queries
- Documentation for CDSCO, US FDA, EMA, and other regulatory authorities
- Post-approval variation documentation
Sample Logistics/Chain-of-Custody
Our sample logistics and chain-of-custody services ensure the integrity and traceability of your samples throughout the testing process. We have established robust procedures for sample handling, storage, and transportation to maintain sample integrity and data quality.
Our Sample Logistics Services Include:
- Secure sample collection and transportation
- Temperature-controlled shipping and storage
- Sample tracking and chain-of-custody documentation
- Barcode-based sample management system
- Long-term sample storage and retrieval
- Sample stability monitoring
- Sample disposal as per regulatory guidelines
- International sample logistics coordination
Ready to Get Started?
Contact us today to discuss your specific laboratory service needs and how Reddy Anna can support your pharmaceutical development projects.