Director Speech

Manish Gajera

Jaydeep Patel

Medilane Healthcare Pvt. Ltd. started its journey in the year 2017 as a leading trader of Active Pharmaceuticals Ingredients, Botanical Extracts & Food additives. Now with five years of unity, extreme hard work and never-ending desire to serve best quality and innovative product to our customers, we are proud to established us as a manufacture with our new manufacturing facility located in surat, India to bring products to the market faster with continuous improvement and innovation.

About Our Company

Medilane Healthcare Pvt. Ltd. Establish in the year 2017 with vision on the development and production of API and specialty chemicals which complies REACH legislation.

We recognize the evolving requirements of the active pharma ingredients markets and aligns itself by providing unique and customized solution-based products.

As a manufacturer of API, the company continuous to follow the quality management systems & global chain management with tremendous effort, patience and dedication in the pharma industry to delivery the innovative solutions. That will cater to this dynamic market.

Our strength lies in our people, with over 25 skilled individuals spread across our manufacturing facilities and corporate office founded and managed by an experienced team of professionals with technical expertise and decades of industry experience.

OUR VISION

Our vision is to become one of the leading global Pharmaceutical API manufacturer & Exporter of quality pharmaceutical API by excelling in the fields of research, regulatory and manufacturing.

OUR MISSION

To create value through superior, pharmaceutical products and operate as a responsible company. Building trust and respect of our valuable customers and employees using science, technology and sustainable processes in harmony with the environment.

OUR Quality policies

  • Standard condition of production and up to date technology ensure consistently high product quality with customer satisfaction.
  • Our APIs are specified and analyzed according to relevant pharmacopoeias and Enterprise standards. To this end all the raw materials, intermediates, APIs, auxiliary materials and packing materials are carefully screened to confirm current GMP norms.
  • Well-equipped quality control laboratory.
  • We have highly qualified staff which are dedicated for all over QC instrument handling and documents preparation.
  • The quality system as defined in Schedule M, Schedule L, ICH Q7 & TRS guidelines.
  • Leading process validation, cleaning validation and analytical method transfers & process technology.
  • Regular evaluation, calibration and monitoring of instruments and equipments.
  • Preparation review and approval of SOPs, protocols and reports.
  • Issuance, retrieval, archival and control of documents.
  • Ensuring GMP compliance of the facility.

Safety Policies

  • Proper measures are in place to avoid accidents and safe handling of various processes.
  • All workers have been provided eye protection and other personal protective equipment (PPE).
  • We regularly check that all equipment is safe to use.
  • We take care about health condition of all our worker on regularly basis with medical checkup.
  • We always avoid over-time work load of our workers and giving them some kind of empowerment for maintaining our quality of products.