ABOUT
SUKTAS
SUKTAS, a consultancy firm established under the Company Act, 2013 of the Government of India in November 2022, is a leading provider of comprehensive consultancy services. SUKTAS offers global solutions across a diverse range of industries, including Pharmaceuticals, Biopharmaceuticals, Medical Devices, Foods, Beverages, Cosmetics, and Testing Laboratories. Our expertise ensures compliance with the most stringent regulatory requirements.
At SUKTAS, we deliver integrated solutions for all your GMP, Quality, Patent, Regulatory, and Engineering needs. Our services encompass pharmaceutical manufacturing, including API production, oral dosage formulations, injectables, dry powders, specialty chemicals, R&D, pilot plants, and facilities for biopharmaceuticals, and healthcare products including oncology, hormones, and steroids.
We stay at the forefront of technological advancements and regulatory updates in the pharmaceutical industry, ensuring our clients benefit from the latest technologies, machinery, and products. SUKTAS is committed to bridging the gap between your pharmaceutical manufacturing aspirations and their realization, providing a seamless path from vision to execution.
Our end-to-end and handholding services encompass extensive reference to the following standards and guidelines:
- USFDA
- MHRA, EMEA
- WHO
- PIC/S
- ICH
- TGA
- ANVISA
- Health Canada
- Japan MHLW
- DBT, RCGM, IBSE
- ROW / Country-specific Regulations
- ISO 13485/ CE, ISO 17025/ NABL, ISO 9001
- FSSAI

OUR CAPABILITIES
Pharmacovigilance
Comprehensive pharmacovigilance services provided, ensuring drug safety and compliance with regulatory requirements globally.
QMS and GMP Documentation
Establishing quality management policies that define the organization's overall approach to achieving quality excellence.
Detailed Engineering
Leveraging 23+ years of experience to facilitate project design, execution, and management for greenfield developments.
Regulatory Support
Offering expert regulatory advice and strategies to navigate complex compliance requirements effectively.
Training
Training includes audio and video classroom sessions to comprehensively understand key concepts and methodologies.
Intellectual Property Rights
Delivering prior art searches, patent specification drafting, filing, and prosecution services for patent applications.
Formulation, Analytical development, and Stability
Supporting analytical and product development needs through our experienced associate company partners.
Qualification & Validation
Offering onsite/offsite qualification services for pharmaceutical facilities, cleanrooms, equipment, and laboratory instruments.
Academic Services
Organizing panel discussions featuring industry leaders on topics like drug development pipelines or emerging pharmaceutical technologies.
Our Clients











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