From regulatory readiness to implementation
Structured professional support for pharmaceutical, nutraceutical, herbal and cosmetic businesses across regulatory documentation, QA/GMP systems, R&D, product-development records and company-specific formats.
Choose the support route that matches your project
DRAP Regulatory & Compliance
Regulatory gap assessment, application-document review, compliance planning and structured support for regulated businesses.
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E-Dossier Preparation
Structured organization of administrative, technical, quality, stability and artwork documentation for submission readiness.
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eAPP Preparation Support
Data organization, supporting-file readiness and structured preparation before entry or upload into the applicable DRAP workflow.
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QA, GMP & SOP Systems
Controlled-document systems for QA, production, warehouse, QC and support departments, including SOPs and implementation records.
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R&D & Product Development
Formulation development, technical records, scale-up documentation and product-development support across regulated product categories.
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Custom Format Development
Company-specific BMR, BPR, MFR, COA, specifications, validation formats, trackers and controlled documents.
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Practical, structured and reviewable support
Run a Regulatory Health Check
Use the free readiness check to identify likely documentation gaps before moving into a detailed professional review.
Request a tailored project review
For combined regulatory, QA/GMP, documentation or R&D requirements, contact Naturegen Lab for a company-specific scope.
