Our Services
Comprehensive laboratory services tailored to your needs
Services Overview
Rd Support offers a comprehensive range of laboratory services to support pharmaceutical, biotechnology, and healthcare industries. Our state-of-the-art facilities and expert team ensure high-quality, reliable results that meet regulatory standards.
Analytical Testing
Comprehensive analytical testing services using advanced instrumentation and methodologies.
Formulation Development
Expert formulation development services for various pharmaceutical dosage forms.
Stability Studies
Comprehensive stability studies to determine product shelf life and storage conditions.
Bioequivalence Support
Scientific support for bioequivalence studies and clinical research.
Contract Research
Customized research services to support your product development needs.
Regulatory Documentation
Expert assistance with regulatory documentation and submission requirements.
Analytical Testing
Our analytical testing services utilize state-of-the-art instrumentation and validated methodologies to provide accurate and reliable results. Our team of experienced analysts ensures that all tests are performed according to established protocols and quality standards.
Our analytical testing services include:
- Raw material testing and characterization
- Finished product analysis
- Method development and validation
- Impurity profiling and identification
- Dissolution testing
- Particle size analysis
- Chromatographic analysis (HPLC, GC, etc.)
- Spectroscopic analysis (UV-Vis, IR, etc.)
Formulation Development
Our formulation development services are designed to help you develop stable, effective, and manufacturable pharmaceutical products. We combine scientific expertise with practical knowledge to create formulations that meet your specific requirements and regulatory standards.
Our formulation development services include:
- Pre-formulation studies
- Excipient compatibility studies
- Prototype formulation development
- Process optimization
- Scale-up support
- Technology transfer
- Formulation of various dosage forms (tablets, capsules, injectables, etc.)
- Reformulation and product improvement
Stability Studies
Our stability studies are designed to determine the shelf life and recommended storage conditions for pharmaceutical products. We conduct studies in accordance with ICH guidelines and regulatory requirements to ensure the quality, safety, and efficacy of your products throughout their lifecycle.
Our stability studies services include:
- Accelerated stability studies
- Long-term stability studies
- Intermediate stability studies
- Photostability studies
- Forced degradation studies
- In-use stability studies
- Stability protocol development
- Stability data analysis and reporting
Bioequivalence/Clinical Support
We provide scientific support for bioequivalence studies and clinical research to help you demonstrate the therapeutic equivalence of your products. Our team works closely with clinical research organizations to ensure that all analytical aspects of bioequivalence studies are conducted according to regulatory requirements.
Our bioequivalence support services include:
- Bioanalytical method development and validation
- Sample analysis for bioequivalence studies
- Pharmacokinetic data analysis
- Bioequivalence study design consultation
- Clinical trial material preparation
- Stability testing of clinical trial samples
- Documentation support for clinical studies
Contract Research
Our contract research services are tailored to meet your specific research and development needs. We offer flexible engagement models that allow you to leverage our expertise and infrastructure while maintaining control over your projects.
Custom Research Projects
We undertake custom research projects based on your specific requirements, from early-stage research to product optimization.
Collaborative Research
We collaborate with academic institutions and industry partners on research projects of mutual interest, bringing together diverse expertise and resources.
Technology Transfer
We provide comprehensive technology transfer services to help you implement new technologies or transfer existing ones between different sites.
Regulatory Documentation Support
Our regulatory documentation support services help you navigate the complex regulatory landscape and prepare high-quality documentation for regulatory submissions. Our team has extensive experience with Indian and international regulatory requirements.
Dossier Preparation
We assist in preparing comprehensive dossiers for regulatory submissions, including CTD (Common Technical Document) format.
Method Validation Reports
We prepare detailed method validation reports that comply with regulatory requirements and scientific standards.
Stability Data Documentation
We compile and present stability data in formats suitable for regulatory submissions, including shelf-life determinations.
Regulatory Response Support
We provide assistance in responding to regulatory queries and deficiency letters related to analytical and formulation aspects.
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 follow strict protocols to maintain sample integrity and provide detailed documentation of all sample handling activities.
Sample Collection
We provide guidance on proper sample collection techniques and offer sample collection kits when needed.
Sample Transportation
We arrange for secure transportation of samples under appropriate conditions to maintain their integrity.
Sample Storage
We provide controlled storage conditions for samples, including refrigerated and frozen storage when required.
Chain-of-Custody Documentation
We maintain detailed records of all sample handling activities, ensuring complete traceability from receipt to disposal.
Need Laboratory Services?
Contact us today to discuss how Rd Support can assist with your specific laboratory service needs.