Pharma & Healthcare
Compliance Management Built for Pharma and Healthcare Enterprises
Pharmaceutical companies and healthcare providers operate under layered regulatory requirements. CDSCO, state drug authorities, NABH, clinical trial regulations, pharma marketing codes, data privacy. eQomply brings it all into one system.
The regulatory reality for pharma and healthcare
Regulatory obligations span drug approvals, manufacturing, clinical trials, marketing practices, and patient data. Different functions own different pieces. Central and state regulators add complexity. Most organizations track compliance in silos.
1
Regulations that span the entire value chain
Manufacturing licenses, import permits, clinical trial approvals, pharmacovigilance, marketing code compliance. Each stage of the business has its own regulatory layer.
2
Central and state regulatory complexity
CDSCO sets national standards, but state drug authorities have their own requirements, timelines, and inspection practices. Compliance teams manage both in parallel.
3
Clinical trial and pharmacovigilance obligations
Trial approvals, ethics committee requirements, adverse event reporting, post-marketing surveillance. These obligations run on strict timelines with serious consequences for delays.
4
Patient data and privacy requirements
Healthcare providers handle sensitive patient information. DPDP Act obligations, NABH data security requirements, and consent management add a compliance layer that most systems were not built for.
What changes with eQomply
eQomply is built for the regulatory breadth of pharma and healthcare. Obligations tracked across functions and regulators. Evidence captured as work happens. Audit-ready documentation without the last-minute scramble.
Unified obligation tracking across the value chain
Manufacturing, clinical trials, pharmacovigilance, marketing, data privacy. All obligations in one system. No more function-by-function trackers.
Central and state requirements in one view
CDSCO and state drug authority requirements mapped and tracked together. Visibility into compliance status across jurisdictions.
Clinical trial and pharmacovigilance workflows
Trial approvals, ethics committee submissions, adverse event reporting. Deadlines tracked, evidence captured, escalations surfaced automatically.
DPDP and patient data compliance
Data protection obligations mapped to healthcare operations. Consent tracking, data subject requests, and privacy documentation in one place.
Evidence captured as work happens
Approvals, attestations, inspection records, training completions. Evidence logged at the source, timestamped, and linked to the relevant obligation.
Inspection and audit readiness
When CDSCO inspections or NABH assessments begin, evidence already exists. Complete, organized, and exportable.
Use Cases
How this works in practice
A new regulation on import licensing is published. eQomply maps it to affected functions, assigns tasks to owners, and tracks completion. Regulatory affairs and compliance teams see the same status. No email chains required.
Inspection notice arrives. Instead of weeks of document assembly across manufacturing, quality, and regulatory affairs, your team pulls reports from eQomply. Evidence is already linked to requirements. Gaps identified before the inspector asks.
Internal audit reviews clinical trial documentation. Ethics committee approvals, informed consent records, adverse event reports. All evidence pulled from eQomply. Timestamped, complete, traceable to source.
See how eQomply works for pharma and healthcare
A walkthrough tailored to your regulatory environment.