Audit-Ready Quality & Compliance Solutions for GxP Environments
Our Quality & Compliance services support pharmaceutical, biotech and medical device organizations in meeting global regulatory expectations. We provide independent audits, inspection readiness, SOP development and ongoing compliance oversight — ensuring your processes remain consistent, compliant and audit-ready at all times.
- Quality & Compliance
Service Overview
Quality and compliance define the foundation of every life-science operation.
At Exsources, we support organizations in building strong, scalable and regulatory-aligned quality frameworks across GCP, GVP and GMP domains.
GCP / GVP / GMP Audits
Independent audits conducted by senior experts with deep regulatory understanding and global experience.
Inspection Readiness Programs
From gap assessments to mock inspections and corrective action planning, we help you prepare with confidence for any regulatory review.
SOP Development & Optimization
Creation, review and harmonization of SOPs to ensure clarity, alignment and consistency across departments and teams.
Vendor Qualification & Oversight
Comprehensive evaluation and ongoing monitoring of external vendors to ensure performance and compliance with global standards.
- Why Choose Us
Regulatory Expertise
Our specialists understand international regulatory requirements and ensure alignment across all processes and documentation.
Independent Perspective
We deliver objective evaluations and identify risks early — helping teams strengthen quality systems efficiently.
Structured & Transparent Approach
Clear documentation, defined checkpoints and detailed reports ensure accuracy and accountability at every step.
Audit-Ready Delivery
All support is designed with inspection readiness in mind — minimizing findings, reducing risk and enhancing data integrity.
- Understanding Our Quality & Compliance Support
FAQ
What types of audits can you perform?
Can you help us prepare for regulatory inspections?
Yes. We offer full inspection readiness programs including gap assessments, CAPA planning, pre-inspection training and mock audits.
Do you develop or review SOPs?
Absolutely. We create, optimize or harmonize SOPs to ensure clarity, consistency and full regulatory alignment across all departments.
How do you handle vendor qualification?
We assess vendor capabilities, review quality systems, perform remote or on-site audits and provide ongoing performance oversight.
Is your support suitable for small teams or only larger organizations?
Our model is flexible — we support small biotech start-ups, mid-size companies and global organizations equally.