Precision Beyond Expectations
Innovative, secure, and customized services for Pharmaceuticals, CROs and Investigator Sites—delivered with excellence, integrity and measurable value
13+
annually
Proven Excellence
140+
Trusted Partnerships
What Sets Us Apart
- Always Audit-Ready
- SOP-Driven Delivery
- Regulatory-Focused Execution
- Data Integrity Assured
Built for Compliance. Trusted for Delivery.
Built for Compliance
- Audit-ready processes
- Clinical research expertise
- Secure, traceable operations
Experienced Teams
Our leadership and operational teams bring decades of combined experience in clinical research, quality systems and regulated service delivery. This depth ensures informed decision-making, risk-controlled execution and consistent service quality across all engagements.
- Proven experience in regulated environments
- Strong understanding of sponsor, CRO and site needs
- Audit-facing and inspection-ready mindset
Tailored Services
Each service engagement is structured based on defined project scope, regulatory expectations, timelines and operational requirements to ensure controlled delivery without unnecessary complexity or risk.
- Project-specific execution models
- Regulatory-aligned workflows
- Controlled timelines and outputs
SOP-Driven Approach
All services are executed through documented SOPs, controlled workflows, and quality checks designed to maintain consistency, traceability and readiness for internal or external audits.
- Documented SOP framework
- Traceable execution steps
- Inspection-ready documentation
Secure & Confidential Operations
Confidentiality and data protection are embedded into daily operations through access-controlled systems, secure infrastructure and disciplined handling of sensitive clinical and regulatory information.
- Access-controlled environments
- Secure data handling practices
- Confidentiality-focused operations
Excellence with Integrity and Value
Excellence
We consistently pursue high standards across services by combining domain expertise, disciplined execution and quality-focused processes that support regulated clinical research environments.
Integrity
We act responsibly and transparently in every engagement, safeguarding confidentiality, data security and ethical conduct while honoring commitments to clients and stakeholders.
Value
We grow responsibly by strengthening capabilities, developing people and maintaining independence—ensuring long-term stability without compromising compliance or service quality.
Specialized Clinical Research Support Services
Language Translation Services
Archival Services
Instrument Rental Services
30%
80%
78%
Meet Our Leaders
Our Journey
CliniApps was established in 2012 in Ahmedabad with a clear focus on supporting clinical research through specialized Language Translation services. From the beginning, the emphasis was on accuracy, confidentiality, and regulatory alignment to meet the demands of clinical documentation and investigator-facing materials.
During this phase, CliniApps built a strong base of native-language experts and developed workflows designed specifically for regulated research environments, laying the groundwork for long-term trust and reliability.
Key Highlights
- Company established in 2012
- Language Translation Services initiated
- Clinical and regulatory documentation support introduced
As clinical programs became more complex, CliniApps expanded its capabilities by initiating True Calibration Services (Truecal) in 2014. This marked an important step toward supporting technical compliance and operational accuracy within regulated environments.
In 2016, Truecal achieved NABL Accreditation, reinforcing structured quality systems, SOP-driven operations and consistent service reliability. This phase strengthened CliniApps’ credibility as a compliant and dependable service provider for regulated industries.
Key Highlights
- True Calibration Services launched (2014)
- NABL Accreditation achieved (2016)
- Formal quality systems and SOPs implemented
To support long-term regulatory requirements and inspection readiness, CliniApps introduced third-party archival services in 2021. This expansion addressed the growing need for secure, compliant document storage within clinical research.
In 2024, CliniApps further strengthened this capability by establishing a state-of-the-art archival facility in Gandhinagar, designed with access control, security and scalability in mind. This phase reflects CliniApps’ readiness to support global sponsors, CROs and long-term clinical programs.
Key Highlights
- Third-party archival services introduced (2021)
- Secure, access-controlled archival infrastructure implemented
- Gandhinagar archival facility established (2024)
Focused Support for Regulated Industries
Pharmaceutical Companies
Clinical Research Organizations (CROs)
Pharmacovigilance Organizations
Medical Device Companies
Built for Regulated Industries
Corporate Office
Archival Facility
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