TOTALRegulatory
End to End & Integrated Functional Services
From Molecule to Market - Seamless Regulatory Support at Every Step for Global Biopharmaceutical Enterprises
Simplify End-to-End Pharmacovigilance Operations by combining People, Process, Technology, Automation & Quality
TOTALRegulatory is Techsol Life Sciences’ proprietary regulatory business solutions methodology, purpose-built to support biopharmaceutical, vaccine, cell therapy, and gene therapy companies throughout the entire product lifecycle from early development to market authorization and post-approval compliance.

Unlike traditional models, TOTALRegulatory delivers a fully integrated, end-to-end regulatory framework that aligns strategy, operations, and technology. Our approach combines deep domain expertise with smart regulatory planning, seamless global submissions, and proactive lifecycle management. A key differentiator lies in our ability to conduct detailed regulatory gap analyses and produce globally compliant, submission-ready documentation that adheres to the highest standards of quality, compliance, and risk mitigation. By leveraging digital tools and process automation, TOTALRegulatory ensures that sponsors are always ahead of evolving regulatory expectations.
Key Service Highlights
- Develop global regulatory strategies (FDA, EMA, EU MDR/IVDR, MHRA, APAC, ROW) to support development and market entry
- Conduct regulatory due diligence, including gap/risk assessments and support for licensing or acquisitions
- Analyze competitors and predicate products to guide submission strategy and regulatory positioning
- Provide lifecycle regulatory support: pre-IND/IDE, IND/IDE, NDA/BLA/ANDA, PMA/510(k), and post-marketing phases
- Author and compile high-quality CMC dossiers (Modules 2 & 3), DMFs, and CTD/eCTD submissions
- Manage Health Authority interactions, including submission responses, briefing books, and meeting support
- Execute complete publishing and submission workflows: planning, compilation, validation, and electronic gateway submission
- Deliver global labeling compliance services: SPC, USPI, local language labeling, artwork review, and SPL conversions
- Provide expert regulatory medical writing for clinical/non-clinical sections, CO, NCO, summaries, and PDE reports



Key Benefits
- Frees up internal teams for strategic work - eliminates up to 60% of the manual effort
- Reduces errors and inefficiencies
- Ensures compliance with global regulations and best practices
- Enables centralized oversight and real-time monitoring
- Seamlessly integrates with your existing systems
Salient Features of Service Delivery
- Comprehensive, end-to-end regulatory lifecycle management and standalone services with customizable engagement models
- Full-spectrum regulatory services integrated with technology platforms
- Flexible resource deployment through regulatory professional services, FTE-based insourcing, or hybrid engagement models
- Direct regulatory liaison support, including strategic communication and response to Health Authority (HA) queries and deficiency letters
- All service models are powered by real-time regulatory intelligence and AI-driven automation to enhance speed, compliance, and decision-making
- Fully auditable and compliant with global regulatory standards (FDA, EMA, MHRA, etc.)
- Centralized project governance ensures consistency, risk mitigation, and transparency
- 24x7 regulatory operations support with proactive issue management
- Positioned as a strategic regulatory partner and extended team to enable faster approvals and sustained compliance across markets

Latest Relevant Case Studies

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Latest Relevant Case Studies

May 1, 2025
Specialized Regulatory Writing Solutions for Clinical Overviews in Combination Therapy Submissions

April 29, 2025
Developing a complex clinical trial Protocol for a CNS-based Psychiatric product …

June 10, 2025
Case study on regulatory strategy development and dossier submission support
Latest Relevant Insights

July 12, 2023
Mastering Medical Device Registrations: A Guide to Navigating Regulatory Pathways

June 21, 2021
Evolution in Global Pharmaceutical Regulatory Landscape & Notable Changes for Sponsors

June 5, 2021
Emerging Trends in Regulatory Affairs by Adapting to Latest Technological Advancements