The combined advantage of experience, expertise, low cost and our excellent partnership with the best manufacturers in India. Emerging as Leading CMO/CMSO organization, we bring unparalleled value to our partners by setting new benchmarks in contract manufacturing services. , we focus on end-to-end solutions, offering seamless integration of product development, manufacturing, and supply chain management.
Our tie-ups with the best, in the industry for most category of formulations ensure that we deliver excellence at every stage. We offer all types of dosage formulations like SVP, LVP, dry powder/liquid injections, oral solid dosage forms, soft gels, and oral liquid dosage forms.
Our diverse product range extends beyond pharmaceuticals to include surgical and medical disposables, medical devices, orthopedic implants, and diagnostic kits. This breadth of offerings highlights our capability to address a wide array of healthcare manufacturing needs with precision and efficiency.
As pioneers in CMSO, we leverage our expertise, infrastructure, and strategic partnerships to deliver exceptional quality and value, making us a trusted partner in the global healthcare industry.
Diverse product range covering surgical and medical disposables and Medical devices, Ortho implants diagnostic kits.
With our state-of-the-art warehouse facility at Bhiwandi, we are specialize in efficient supply chain management for cold storage products, employing a system designed to optimize the handling and preservation of temperature controlled goods. Our commitment to excellence ensures the timely and reliable delivery of products, allowing our customers to receive their cold storage items in optimal condition. By adhering to stringent safety standards throughout the entire logistics process, we guarantee the integrity of our products while maximizing operational efficiency.
We ensure that products marketed are specifically designed to meet the global regulatory requirements, uphold patient safety, and maintain the trust of healthcare professionals and consumers.
Additionally, we utilize third-party testing to validate product safety and efficacy, ensuring that all our products meet the highest standards. Our expert business development team is dedicated to understanding market needs and driving strategic growth, while our PPIC team ensures smooth production planning, inventory control, and on-time delivery. Our dedicated regulatory affairs team ensures compliance with all local and international regulations, managing labeling, approvals, and documentation.
Furthermore, we offer ISO/CE-certified diagnostic and surgical devices, meeting global standards for medical device safety and quality.
Above all, our unwavering focus on patient safety is embedded in every aspect of product development, from raw material processing to the release of finished goods, ensuring the highest level of trust and reliability for healthcare professionals and consumers.
We ensure our products are manufactured at facilities that are GMP certified & validate manufacturing processes to ensure consistency and compliance at every stage, from raw material processing to finished product release. Comprehensive testing services, including chemical, microbiological, and stability testing, are implemented so our products meet the highest safety and efficacy standards before reaching the market.
We also export Diagnostic and Surgical devices which are of high standard and meet ISO/CE certification and labelling mandate as per the regulatory requirements
Our dedicated team ensure compiling and submitting high-quality CTD, ACTD, and country-specific dossiers, while managing BA/BE studies in compliance with Ministry of Health (MoH) requirements ensuring products meet global standards and navigate approval processes smoothly.
Our services include maintaining updated databases, and reviewing product labeling, packaging, and artwork to meet local regulations. We also offer post-approval support, and regulatory intelligence throughout the product lifecycle.
With our expertise, we provide tailored solutions, strategic guidance, and efficient resolution of regulatory challenges, ensuring timely product approval and compliance.
We provide comprehensive support for international regulatory authority audits, ensuring that pharmaceutical manufacturing facilities meet the stringent requirements of global regulators such as the NDA. TMDA etc.
Our team experts, with extensive experience in international inspections, assists in preparing for audits, coordinating with auditors, and ensuring compliance with all relevant regulations.
We offer expertise in managing documentation, addressing audit findings, and implementing corrective actions to maintain ongoing compliance, helping our vendors navigate the complexities of international standards and successfully pass audits.
The consolidation of multiple shipments is a strategic logistics approach that aggregates smaller shipments into a single, larger shipment, thereby optimizing supply chain efficiency and reducing shipping expenditures. With the state of art of warehouse at Bhiwandi we utilise this methodology to yield numerous benefits, including enhanced cost efficiency, optimized cargo space, expedited transit times, and a diminished environmental footprint. While implementation may present challenges, such as complex supplier coordination, extended lead times, and regulatory compliance, the advantages of shipment consolidation often outweigh these hurdles, particularly for high-volume businesses seeking to streamline their logistics operations.
