Regulatory Services and Compliance
MaxScientific services can assist you in ensuring the quality and acquiescence of your nutraceutical product during its entire lifecycle. From pre-market to post-market reviews, inspection, and compliance, we can shepherd your products through design, labeling, promotion, production, and testing.
Our services include:
Regulatory Affairs
Regulatory affairs are Maxsci’s backbone and we fully understand the complexities of the nutraceutical industry. Our expertise spans all facets and levels of Regulatory Affairs, from early phase & bioanalytical sciences through late phase and post market support.
- Formulation and GRAS applications
- Marketing Applications
- Medical Writing
- eCTD Publishing & Submissions
- Strategic Consulting & Intelligence
- Project Management Support
- Clinical Development Support
- Clinical Research Organization (CRO) Sourcing
- Analytical Development Support
- Bioassay Design & Validation
- Immunoassay Support
- Statistical Analysis & Specification Setting
- Compliance Assurance
Increasingly, life science companies are feeling the pressure of greater scrutiny by regulators, and we are responding by developing sustainable compliance strategies. Whether it’s preparing for an audit, developing a response to an FDA finding, or remediation to an adverse event, Maxsci can help.
Assessments
- Current Good Manufacturing Practice (cGMP)
- Corrective & Preventive Action (CAPA), Investigations & Deviations
- Data Integrity
- Quality System Gap Assessment
- Audits
- Supplier Audits
- cGMP Compliance Audits: Manufacturing, Pilot Plant, Laboratory
- Preparation, Training & Inspection Readiness
- cGMP Fundamentals (Annual Training Required by Regulations)
- Quality System Regulation
- Risk Management
- Investigations, Deviations & CAPA & Root Cause Analysis
- Validation & Technology Transfer
- Purchasing Controls & Supplier Management
- Document Management & Change Control
- Audit Readiness
- Quality Culture & Management Responsibility
- Data Integrity & Good Documentation Practices (GDP) Centered on How the Data is Recorded, How to Correct an Error, and How to Document the Reason(s) for the Error
- Quality Assurance
Maxsci’s Quality Assurance services include assessments, strategy, implementations, staff augmentations, and identification of quality metrics to ensure continuous improvement, aligning with your business needs with your long-term goals through a viable and realistic strategy. Our consultants are quality experts with experience spanning major corporations and start-ups. We know firsthand how to achieve, maintain, and improve quality, and we excel in transferring this knowledge to your organization.
Quality Management System Implementation
- SOP Development
- Document Control Systems
- Change Control
- Laboratory Operations & Control
- Remediation Strategy & Response
Maxsci is widely recognized within the life science industry and global regulatory agencies for its ability to help companies successfully resolve complex regulatory challenges, including remediation.
With a proven track record of success, we have significant experience with the development of responses to 483 Observations, Warning Letters, Untitled Letters and Consent Decrees.
Regulatory Action
- 483 Response & Remediation
- Warning Letter Response & Remediation
- Consent Decree Response & Remediation
- Oversight Services
- Consulting
- Comprehensive Audits
- Remediation Plan Development & Implementation
- Manufacturing Support
- Re-validation of Existing Equipment & Processes
- Remediation of System Deficiencies Related to, Manufacturing Process, Equipment, or Facility