We are
Ortiv-Q3.
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We are
Experts.
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We are
Research.
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We are
Development.
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Where We Are.
Ortiv-Q3 Research Pvt. Ltd.
Ratna Business Hub, B-202-207, 2nd Floor
Near Sanathal Circle, Sarkhej - Bavia Highway
Ahmedabad, Pin 382 210, India
P Office +91 76 7670 7801
info@ortiv.in
Our Lab.
We have the expertise and knowledge to assist global pharmaceutical companies with their dissolution and release testing needs for different dosage forms. We are experts in in vitro dissolution testing and we can find the best method for various products, such as APIs, tablets, implants, semi solids, and more.
Certified Quality.
Ortiv-Q3 Research is committed to implementing a pharmaceutical quality system that complies with the applicable Good Manufacturing Practice requirements of US 21 CFR Parts 210, 211 and the principles of the ICH Q10 guideline. The laboratory endeavours to continuously review and improve its capabilities and communication in accordance with the requirements of ISO/IEC 17025:2017 to ensure the confidentiality and impartiality of all parties involved.
Your Career.
We welcome all members of our multicultural workforce, whether they are new to the industry or have many years of experience. The cultural diversity of our workforce is one of our greatest assets. We value our employees as our most valuable resource. Each of our team members is empowered to excel through comprehensive training, development and career guidance programmes.
Management
The Ortiv-Q3 leadership team brings decades of laboratory and management experience from various industries together. These diverse backgrounds help Ortiv-Q3 evolve along with technology and continue providing value-added services to its clients.
Dr. Mukesh Kumar
Dr. Mukesh Kumar
Director
Mukesh is a pharmaceutical veteran with expertise in various injectable and ophthalmic dosage forms for regulated markets. He is specially versed in reverse engineering, in vitro /in vivo release studies, and Q3 characterization. He has profound knowledge in formulation development, preclinical evaluation, process development, optimisation, and scale-up of formulations for markets like the USA and Europe.
Pawan K. Gupta
Pawan K. Gupta
Director
Pawan is a pharmaceutical scientist with expertise in various dosage forms like Liposomes, Nanoparticles, Microspheres, Nano-suspensions, emulsions, Semisolids, Transdermal patches, Ophthalmics, Inhalations, Solid & liquid orals. He has vast experience in all functions of analytical department, like method development, validation, tech transfer, stability, regulatory queries, compliance and quality assurance.
Ashish Gupta
Ashish Gupta
Director
Ashish is an established scientist with experience in Analytical R&D. He is experienced in end-to-end product development of complex formulations and APIs in terms of analytical aspects such as development, method validation and transfer, QC testing, and stability studies. His expertise is in Q1/Q2 reverse Engineering and in-vitro Q3 characterization, IVRT method development, and validation of many challenging and complex pharmaceutical dosage forms.
