Rusan Pharma Achieves Global GMP Milestone with PMDA Japan Approval
Rusan Pharma's facilities in Ankleshwar (Gujarat) and Dehradun (Uttarakhand) have successfully secured GMP approval from the PMDA, Japan, one of the most stringent regulatory authorities globally. The approval covers the company's Active Pharmaceutical Ingredient (API) facility in Ankleshwar and its Small Volume Parenterals (Ampoules) Finished Dosage Formulation (FDF) manufacturing line in Dehradun.
Mumbai (Maharashtra) [India], April 20: Rusan
Pharma, a leading pharmaceutical company pioneering pain management, movement
disorder, and addiction solutions worldwide, has achieved a significant global
regulatory milestone with the successful Good Manufacturing Practice (GMP) approvals
from Japan's Pharmaceuticals and Medical Devices Agency (PMDA). This
achievement reinforces the company's commitment to world-class quality,
compliance, and global manufacturing excellence.
Rusan Pharma's facilities in Ankleshwar (Gujarat)
and Dehradun (Uttarakhand) have successfully secured GMP approval from the
PMDA, Japan, one of the most stringent regulatory authorities globally. The
approval covers the company's Active Pharmaceutical Ingredient (API) facility
in Ankleshwar and its Small Volume Parenterals (Ampoules) Finished Dosage
Formulation (FDF) manufacturing line in Dehradun.
Commenting on the achievement, Dr. Kunal Saxena,
Managing Director, Rusan Pharma, said, "I am extremely happy and proud to
share that Rusan has been granted GMP approval from one of the world's toughest
regulatory authorities - Japan's PMDA - for our API facility in Ankleshwar,
Gujarat, and our Finished Dosage Formulation (FDF) ampoule manufacturing line
in Dehradun, Uttarakhand. This achievement places Rusan among the very few
companies worldwide to have both API and FDF facilities GMP-approved by the
Japanese authority, further strengthening our position as a trusted partner for
high-quality pharmaceutical development, manufacturing and licensing partner.
It reflects the dedication of our teams, the robustness of our systems, and our
unwavering focus on delivering world-class quality to patients and partners
across the globe."
This milestone marks a significant step in Rusan
Pharma's global growth journey, enhancing its ability to cater to highly
regulated markets such as Japan while expanding its portfolio of high-quality
pharmaceutical offerings.
Rusan Pharma continues to invest in strengthening
its manufacturing infrastructure, quality systems, and regulatory preparedness,
driven by a long-term vision to be a trusted global partner in pharmaceutical
manufacturing and healthcare delivery.
About Rusan Pharma:
Rusan Pharma Pvt Ltd. is an integrated global
pharmaceutical company and market leader that specialises in the treatment of
Addiction and Pain Management. They offer a complete range of super-specialised
products in India and globally. Rusan indigenously develops, manufactures, and
markets novel APIs and finished formulations and is one of the few notified companies,
which is allowed imports of Narcotic Raw Materials (NRM) such as Thebaine,
Oripavine, Codeine and Morphine for the purpose of manufacturing various APIs
and finished formulation in India and then re-exporting to global markets. Over
the years, Rusan has closely worked with Indian and global institutions such as
NACO, UNODC, UNOPS, Global Fund, and Ministries of Health to launch Opioid
Substitution Therapy in various emerging markets.
Rusan Pharma's strength lies in innovation of New
Drug Delivery Systems (NDDS) such as transdermal patches, implants, depot
injections. Rusan was the first company to launch Fentanyl, Buprenorphine and
Nicotine Transdermal Patches in India. The company supplies range of products
to countries such as India, Canada, Europe, UK, Russia, CIS, South Africa and
other South-East Asian countries. Rusan's API and finished formulation
manufacturing facilities hold GMP accreditations such as USFDA, Health Canada,
EU, TGA (Australia), SAHPRA (S.Africa), RUSSIA, PIC/S (UKRAINE), ANVISA
(Brazil) UAE and many more.
(ADVERTORIAL DISCLAIMER: The above press release
has been provided by VMPL. ANI will not be responsible in any way for the
content of the same.)