Biotech & Pharma preparing for ISO 27001 face the same challenge: protecting research data and clinical information. MDRwatchdog makes it manageable with continuous monitoring and automated evidence.
Book a 15-minute review →Biotech & Pharma are increasingly asked to demonstrate ISO 27001 readiness. The obligation stems from protecting research data and clinical information, and ISO 27001 (ISO/IEC 27001:2022 Annex A (93 controls)) is how it is measured. MDRwatchdog monitors your endpoints, cloud, and identity around the clock and maps that telemetry to the framework's controls.
You receive your Annex A control status, Statement of Applicability support, gap remediation, ISMS evidence generated from live evidence. Controls the platform can prove are marked as evidenced; the rest are flagged for attestation. The underlying audit trail is hash-chained and independently verifiable, so what you hand an assessor is defensible, not a self-graded checklist.
Whether you are early in your ISO 27001 journey or refreshing evidence for a renewal, the platform keeps you assessment-ready.
ISO 27001 is certified or determined by an accredited certification body; we get you ready and keep you ready.
Biotech & Pharma become ISO 27001 ready by demonstrating the controls in ISO/IEC 27001:2022 Annex A (93 controls). MDRwatchdog monitors your environment and generates your Annex A control status from live evidence, flagging gaps for remediation.
ISO 27001 is measured against ISO/IEC 27001:2022 Annex A (93 controls). For biotech and pharmaceutical companies, the obligation typically stems from protecting research data and clinical information. The deliverables include Annex A control status, Statement of Applicability support, gap remediation.
No. ISO 27001 is certified or determined by an accredited certification body. MDRwatchdog provides the readiness and evidence to prepare you; it is not a certification and not legal advice.
MDRwatchdog provides security monitoring and compliance evidence to support readiness. It is not a certification and not legal advice. Certification and formal audits are performed by the appropriate authorized bodies (a C3PAO for CMMC, a licensed CPA firm for SOC 2, an accredited body for ISO 27001).