Why Choose Us?
Commitment to Quality
At Super Nova Life Drugs Private Limited, quality is the cornerstone of our operations. Our robust Quality Management System (QMS) complies with global regulatory guidelines, including WHO-GMP, ICH, PIC/s, and Revised Schedule-M, ensuring that every product meets the highest standards of purity, identity, safety, and efficacy.
- Quality Control (QC): Our QC team rigorously tests raw materials, intermediates, and finished products to guarantee only the best medicines reach our customers.
- Quality Assurance (QA): An independent QA Department ensures compliance with cGMP and cGLP practices, oversees the approval of key documents, and conducts in-process checks, internal audits, and vendor qualifications.
- Global Compliance: Regular audits, self-inspections, and vendor evaluations ensure adherence to regulatory requirements and continuous improvement across all operations.
MR. PRADEEP SHARMA
DIRECTOR – QUALITY CONTROL & PLANT HEAD
Advanced Quality Systems and Processes
01.
Core QA Elements:
- Clear roles and responsibilities for all employees.
- Comprehensive SOPs and work instructions.
- Effective systems for handling complaints, recalls, and deviations.
- Thorough investigations of OOS/OOT results and management of CAPAs.
02.
Audit Programs:
- Internal Audits: Conducted semi-annually or during critical events to ensure cGMP compliance.
- External Audits: Welcoming inspections by regulatory authorities and customers, with prompt corrective actions.
03.
Vendor Management:
- Vendors are rigorously evaluated through detailed questionnaires and on-site audits.
- An annually updated Approved Vendor List (AVL) ensures supply chain integrity.
Advanced Quality Systems and Processes
01. Core QA Elements
- Clear roles and responsibilities for all employees.
- Comprehensive SOPs and work instructions.
- Effective systems for handling complaints, recalls, and deviations.
- Thorough investigations of OOS/OOT results and management of CAPAs.
02. Audit Programs
- Internal Audits: Conducted semi-annually or during critical events to ensure cGMP compliance.
- External Audits: Welcoming inspections by regulatory authorities and customers, with prompt corrective actions.
03. Vendor Management
- Vendors are rigorously evaluated through detailed questionnaires and on-site audits.
- An annually updated Approved Vendor List (AVL) ensures supply chain integrity.
Formulation and Development (F&D) Department
Our Formulation and Development (F&D) Department is dedicated to designing and developing innovative, patient-centric medicines. The F&D team bridges the gap between drug discovery and commercialization by:
- Creating safe, effective, and user-friendly formulations.
- Ensuring the stability, bioavailability, and therapeutic efficacy of APIs.
- Testing and analyzing formulations for quality, stability, and shelf life.
- Monitoring pilot-scale batches to ensure consistency before commercial production.
- Developing cutting-edge drug delivery systems, such as sustained-release tablets and transdermal patches.
This department ensures that our products meet scientific, regulatory, and patient-centric requirements.
Manufacturing Excellence
Our manufacturing facility is equipped to produce a wide range of pharmaceutical formulations, including tablets and bilayer tablets. To ensure operational precision and quality, we collaborate with external experts for:
- Pest and rodent control.
- Calibration of measuring instruments.
- HVAC validation.
- External training programs.
- Medical services.
- Laboratory testing for samples requiring specialized analysis outside our in-house capabilities.
Clinical Development
Pioneering clinical development to ensure safe, effective, and patient-focused pharmaceutical solutions.
Regulatory & Access
Streamlining regulatory compliance and global market access to deliver trusted medicines worldwide.
Biotech
Advancing biotechnology innovations to develop cutting-edge therapies for a healthier future.
Functional Service
Regulatory, and quality operations to ensure efficient and compliant drug development.
Compliances and certifications
Compliances and certifications
