Institutional Governance & Compliance

Integrity as a Core Institutional Value

We maintain the highest global standards of healthcare research ethics, data protection, and professional compliance. Our operational framework is engineered for absolute transparency and audit-ready precision.

The Architecture of Compliance

The Architecture of Compliance

Play Motion Element

PDP Alignment

Strict adherence to the Indonesian Personal Data Protection (PDP) law and global HIPAA-grade encryption standards for all sensitive information.

GCP Standards

Execution of all medical and clinical research according to Good Clinical Practice (GCP) guidelines to ensure respondent safety and data validity.

Methodological Audit

Transparent, audit-ready documentation for every research touchpoint, from respondent recruitment to final analysis and reporting.

Institutional Ethics

Adherence to ESOMAR and EphMRA international codes of conduct, ensuring the highest level of professional and ethical research standards.

Data Infrastructure

Security & Privacy

Our data ecosystem is built on the principle of 'Privacy by Design,' utilizing multi-layered security protocols to protect sensitive healthcare and consumer data.

End-to-End Encryption

All data in transit and at rest is protected by AES-256 bit encryption.

Isolated Data Silos

Strategic isolation of PII (Personally Identifiable Information) from research datasets.

Access Governance

Strict role-based access controls and multi-factor authentication for all internal systems.

Medical Ethics

Adverse Event (AE) Reporting Protocols

As a specialized healthcare research firm, we maintain rigorous protocols for identifying and reporting Adverse Events (AE) and Product Complaints (PC) according to global pharmaceutical standards.

AE Identification

All field teams and moderators are trained to identify and flag potential adverse events in real-time.

24-Hour Reporting

Guaranteed reporting of verified AEs to pharmacovigilance departments within 24 hours of discovery.

PV Compliance

Continuous training and certification of all operational staff in Pharmacovigilance (PV) compliance.

RFP & Tender Support

Astha Insights provides full compliance documentation and technical descriptions for corporate tender submissions and government RFP processes.

Validated healthcare research provider status
Demonstrated local fieldwork infrastructure
Financial transparency and professional liability
Conflict of interest disclosure protocols

Non-Promotional Declaration

"Astha Insights strictly separates research activity from any commercial promotion. Our engagement with physicians is solely for the purpose of objective data collection and strategic intelligence gathering, ensuring no influence on prescription behavior or institutional procurement."