Yes. We support security assessments, access control improvements, logging and monitoring design, backup and recovery readiness, supplier oversight, and remediation planning for systems that support GxP processes. Work is planned to avoid unnecessary disruption to validated states.
Cybersecurity for Pharmaceuticals & Life Sciences
We help pharmaceutical manufacturers, biotech companies, laboratories, CROs, CDMOs, and life sciences organizations protect research data, GxP systems, clinical operations, and regulated business-critical environments.
Built for Regulated Research, Clinical, and Manufacturing Environments
Pharmaceuticals and life sciences organizations depend on digital systems across discovery, laboratory work, clinical trials, quality, manufacturing, pharmacovigilance, and distribution. A cyber incident can delay trial milestones, interrupt batch release, damage data integrity, or disrupt the flow of medicines and therapies.
The sector protects highly valuable intellectual property, patient and trial participant data, formulas, analytical results, and supplier records. Attackers often target credentials, research repositories, cloud workloads, manufacturing networks, LIMS, MES, QMS, CTMS, eTMF platforms, and third-party connections that support regulated processes.
Security work must fit GxP expectations, EU GMP Annex 11, 21 CFR Part 11 where applicable, GDPR, ISO/IEC 27001, and NIS2 for in-scope entities. B2B Cyber helps translate these requirements into practical controls, evidence, access governance, incident readiness, and resilient operating models.
IN A WORLD OF 
THREATS, WE DEPLOY 
EXPERTS TO BUILD YOUR DEFENSE 
Where We Add the Most Value in Pharmaceuticals & Life Sciences
Resilience of GxP and Laboratory Systems
We help secure validated and business-critical systems such as LIMS, MES, QMS, CTMS, eTMF, document repositories, and laboratory platforms. The focus is on access control, logging, backup readiness, change discipline, and protection against disruption without weakening validated states.
Protection of Research Data and Intellectual Property
We support controls around research repositories, collaboration platforms, analytics environments, and cloud workloads that store formulas, study data, compound libraries, genomic data, and regulatory documents. This reduces exposure to theft, unauthorized sharing, and manipulation.
Clinical Trial Data Integrity
We help strengthen security around clinical trial platforms, investigator portals, ePRO, eCOA, IRT, safety databases, and data transfer workflows. The goal is to protect confidentiality, traceability, availability, and auditability across sponsors, sites, vendors, and partners.
Manufacturing and Supply Chain Security
We assess and improve safeguards for production networks, batch-related systems, warehouse processes, remote access, suppliers, and service providers. This helps reduce the risk of manufacturing interruption, data loss, unauthorized change, and delayed product release.
Regulatory Readiness and Security Evidence
We help teams build practical evidence for audits, inspections, internal risk reviews, and management reporting. Support can include control mapping, gap analysis, policy work, supplier oversight, remediation planning, and alignment with relevant standards and regulatory expectations.
Services for Pharmaceuticals & Life Sciences
01
Cybersecurity Experts on Demand & Outsourcing
Quickly strengthen your internal team with specialists who understand regulated environments, GxP systems, clinical operations, manufacturing constraints, and sensitive research data. We provide experts for architecture, identity and access, cloud security, supplier risk, validation-related security work, assessments, and urgent delivery peaks.
02
Security & Compliance Project Delivery
We deliver structured cybersecurity and compliance projects for pharmaceutical and life sciences environments, including GxP system security reviews, EU GMP Annex 11 and 21 CFR Part 11 support, ISO/IEC 27001 alignment, NIS2 readiness where relevant, control implementation, audit preparation, and remediation planning.
03
Managed Security Services
Delegate selected security operations to an external team while keeping clear ownership over regulated processes. We can support monitoring, vulnerability management, access reviews, cloud configuration checks, incident workflows, supplier follow-up, and recurring reporting for critical pharmaceutical and life sciences environments.
Typical Roles We Provide to Pharmaceuticals & Life Sciences Organizations
Life Sciences Security Architect
Cloud Security Specialist
OT Security Specialist
Vulnerability Management Specialist
GxP Security Consultant
IAM or PAM Engineer
Security Project Manager
Data Protection and Privacy Advisor
System Validation Security Specialist
Third-Party Risk Specialist
Incident Response Specialist
Security Awareness Consultant
YOUR BENEFITS
Business Outcomes We Deliver
Why Pharmaceuticals & Life Sciences Organizations Choose B2B Cyber
Life sciences security cannot ignore validation, quality, evidence, and operational constraints. We combine practical cybersecurity expertise with delivery discipline, helping teams move from risk findings to implemented controls that support research, clinical, manufacturing, and regulatory priorities.
Regulated environment focus
We adapt security work to GxP processes, validated systems, data integrity expectations, and the realities of quality-driven organizations.
Flexible engagement model
Use one expert, a focused project team, or recurring managed support depending on your internal capacity, urgency, and target outcomes.
Implementation over theory
We focus on controls, evidence, workflows, and remediation plans that internal teams can use, not generic recommendations that remain unresolved.
Scalable security support
Start with a defined area such as GxP systems, suppliers, or cloud environments, then expand support as risk priorities and workloads change.
Need Cybersecurity
Support for Pharmaceuticals & Life Sciences?
Talk to B2B Cyber about your research data, GxP systems, clinical trial platforms, manufacturing environment, supplier dependencies, and regulatory priorities. We will help define the right scope, specialists, delivery model, and next steps.
Frequently Asked Questions
Can you help with EU GMP Annex 11, 21 CFR Part 11, and audit readiness?
Yes. We help translate relevant expectations into practical security controls, documentation, evidence, and remediation plans. This may include reviews of access, audit trails, change control, data integrity safeguards, system inventories, vendor responsibilities, and incident procedures.
Can support include CROs, CDMOs, laboratories, and technology providers?
Yes. Pharmaceutical and life sciences organizations often rely on external partners for trials, manufacturing, analytics, hosting, and specialist platforms. We help map dependencies, review access paths, define security expectations, assess supplier risk, and prioritize follow-up actions.
Do you provide individual specialists or ongoing managed security support?
Both. We can provide individual experts for internal teams, deliver a defined project, or take responsibility for selected recurring security activities. The model depends on your internal structure, regulated processes, urgency, and the level of control you want to retain.