Welcome to AVQC, Inc.!
We are a Multinational Life Sciences Global Compliance Consulting Firm with 25 + years experience delivering Technical Writing and Validation Services in the Pharmaceutical, Medical Device, Biotechnology and Food Industries.
We comply with FDA, MHRA, TGA, Health Canada, EMEA and ISO 90001, 14971 and 13485.
Call Us For Your Free Initial Consultation!
Our Customer Support, Service and Consultations - are Rated #1 by our customers!
24 hour Service: +1.877.772.6375
We Deliver an Array
of Dependable Compliance Solutions.
We conduct business responsibly and transparently, while utilizing the highest level of quality throughout.
We always utilizes a Strict Code of Business Ethics to be a trusted partner.
We provide an essential, time efficient, and cost-effective service.
We Ensure Your Compliance
We recognize the need to provide quality technical writing services in our highly technical and highly regulated environment as Compliance, Regulatory and Legislative requirements have put high demands on companies to provide documented evidence of procedures, policies and standards.
At AVQC, Inc., we work closely with our clients to capture requirements, develop deliverable schedules, and deliver final high quality documentation on time and on budget.
a Full Range of Services
We deliver a full range of pharmaceutical and medical device consulting services in the areas of compliance and validation to help ensure your firm obtains and maintains GxP-compliance. Click HERE to see a glimpse of some of the services we provide.
Contact Us for Dependable Compliance Solutions.
We are available 24/7 for Domestic & International Clients: +1.877.772.6375
Delivers Quality Service
Our team of professional consultants has decades of experience in a variety of areas in the Pharmaceutical, Medical Device, Biotechnology and Food Industries, serving both domestic and international clients.
We are uniquely qualified to assess your company’s facility, quality system, policies, plans, protocols and procedures, while providing specific advice and expertise to remediate these areas to ensure a successful inspection outcome. We work on-site, remotely, or as a staff augmentation team to suit your needs.
We Offer an Array
of Pharma, Medical Device & Biotechnology
We specialize in the areas of Compliance and Validation to help ensure your firm
obtains and maintains GxP-compliance.
Regulatory Services | Quality & Compliance Services | Validation Services | Technical Services
Regulatory, Quality & Compliance Services
- Strategic Planning for FDA Facility Approval
- Facility and Pre-approval Audits
- 483, Warning Letter and Consent Decree Remediation Projects
- On-site assistance during FDA inspections
- Quality System Development and Implementation
- CAPA Management
- Supplier Controls
- Customized Training Programs
- Batch Record Review
- Audit Prep, Vendor and 3rd Party audits
- Regulatory Submissions
- Equipment Validation
- Computer System Validation
- Cleaning Validation
- Process Validation
- Test Method Validation
- Utilities Validation
- Laboratory Instrument Validation
- Data Integrity Assessments
- Gap Analysis
- Technical and Procedural Remediation
- Functional Requirements, User Requirements, and Design Specifications
- Commissioning Documents, Site Acceptance Tests, Test Plans and Protocols, Protocol Execution and Validation Testing.
- Site Validation Master Plans, Validation Master Plans, and Summary Reports.
- Verification of Piping and Instrumentation Diagrams, Isometric Drawings, and Loop Sheets
- Document Research, Data Analysis, and Feasibility Studies
- Creation, Modification and Revision of Technical Manuals, Training Manuals, Administrative Guides, White Papers & Standard Operating Procedures
Contact Us for Our Full List of Services!
We Provide Quality Compliance Services For All Your Inspection Needs.
We Deliver Quality Compliance Solutions that Exceed Your Expectations.
Schedule Your Consultation - Today
We Respond to Email's Around the Clock.
24/7 Service: +1.877.772.6375
We are available to our Domestic and International clients around the clock. Please leave a detailed message, we respond to requests promptly.