Our Services

At SSK Research Institute, we provide an end-to-end portfolio of services encompassing all areas of clinical research, from biospecimen procurement to trial conduct and regulatory compliance. Our aim is to deliver precision, quality, and value at each touch point.

1. Clinical Operations

We enable trailblazing research in multiple areas of therapeutics with a robust inventory of high-quality human biospecimens that have been procured ethically, including:

  • Infectious Diseases: Hepatitis, Tuberculosis, HIV, Syphilis, Influenza A & B, Human Metapneumovirus (HMPV).
  • Oncology: Types of cancer including breast, lung, pancreas, stomach, urinary bladder, gynecological cancers, and neuroblastoma.
  • Chronic & Metabolic Disorders: Cardiovascular disease, diabetes, metabolic syndromes, endometriosis, and vitamin deficiencies.
  • Tissue Types: Snap-frozen, Fresh, and FFPE (Formalin-Fixed Paraffin-Embedded)
  • Other Specialized Samples: NCFBE (Non-Cystic Fibrosis Bronchiectasis) and others.

2. Site Management

We offer full clinical site management services that make sure the trial is done in an ethical and smooth way. From start-up and site selection to monitoring, our experts guarantee regulatory compliance, robust patient recruitment, and optimal performance of study sites.

3. Medical Writing

Our experienced medical writing staff provides concise, clear, and regulatory compliant documentation, such as:

  • Clinical Study Protocols
  • Investigator Brochures
  • Informed Consent Forms (ICFs)
  • Clinical Study Reports (CSRs)
  • Scientific Publications and Summaries

4. Clinical Data Management

We provide secure and reliable data solutions that enable high-quality results. Our data management services are:

  • Database design and validation
  • Electronic Data Capture (EDC) implementation and maintenance
  • Data cleaning and discrepancy management
  • Statistical programming support
  • Preparation of datasets for regulatory submission

5. Quality Assurance

Our dedicated Quality Assurance (QA) personnel is responsible for ensuring each project is to Good Clinical Practice (GCP), ethical, and regulatory requirements. We perform:

  • Internal audits
  • Vendor and site audits
  • Quality control checks
  • Risk-based monitoring and CAPA implementation

6. Clinical Pharmacology Services

We offer the early and late stages of pharmacology services, so you can make the most out of your trials like:

  • Pharmacokinetic (PK) and Pharmacodynamic (PD) assessment
  • Bioanalytical sample management
  • Protocol-driven sample collection
  • Support for bioequivalence and bioavailability studies

7. Clinical Trials

SSK Research provides complete support for clinical trial design, conduct, and monitoring. We partner with sponsors across phases (I-IV) for guaranteeing studies are conducted:

  • Ethically and safely
  • In regulatory compliance
  • Within budget and timelines
  • Targeted on patient and science-based outcomes

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