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Quality Policy 

AQMED is committed to developing and delivering pharmaceutical and cosmetic products that are of the highest possible quality, effectiveness, and safety as part of our commitment to enhancing peoples health.

We achieve our quality goals by developing, implementing, and maintaining a successful quality management system. We commit to preserving and improving this quality system.
We also follow all applicable laws and rules established by national and international authorities. We adhere to the cGMP guidelines established by WHO.

Our Team 

Mr. Dhaval Vyas: He has extensive knowledge of creating and investigating Finish dosage forms. Additionally, by holding senior management roles in numerous organizations, he was able to prosper and obtain an advantage in the areas of business development, marketing, and export. Over the course of a more than 20-year career, he has guided the our organisation to become world leaders in their niche industries.

Mr. Nilesh Yadav: He has expertise in the development of formulations, problem-solving, compliance, and regulatory concerns. His area of expertise is the research and development of final dosage forms. He assisted in filling more than 50 items in a number of regulated markets, including those in the USA, Europe, and other regions. He has guided the aforementioned organizations as they became world leaders in their respective fields over the course of a more than ten-year career.

Manufacturing Unit 

A cutting-edge production facility Anand in Gujarat is where the AQMED manufacturing plant is located.(Kheda). Our robust R&D facilities, skilled workforce, and well-equipped machinery all help to produce goods that adhere to international standards. In addition, the facility features a robust infrastructure and an environmentally friendly work environment, both of which help to solidify our position as market leaders in the private labelling sector.
Our state-of-the-art production capabilities enable the rapid and reliable development of high-quality products. Since we are dedicated to quality and trust, we work together with our clients to manufacture the best goods in a transparent manner at all production phases.

What Makes Our Manufacturing Plant Stand Out?

  • Our manufacturing unit us 48,500 square feet in size.
  • We have FDA approved R.C.C.s 19,000 square foot production plan.
  • We capable of producing goods that fulfil the USFDA, ISO, and cGMP requirements for quality and manufacturing.
  • All manufacturing and filling areas are maintained under class D (HEPA Filters) with epoxy flooring, and all production area walls are covered with clean room partitions in order to maintain cleanliness and hygienic conditions.
  • There are filling chambers and air locks for man and material access in each manufacturing area.
  • Critical areas employ biometric access control to stop unauthorised personnel from entering.
  • Examples of utilities include an effluent treatment facility, diesel generators, and compressed air systems.
  • Each zone has its own AHUs (Air Handling Units), dehumidifiers, and dust extraction systems.
  • Important processing operations are separated for each zone to avoid cross-contamination.
  • Construction of a state-of-the-art testing and product development laboratory.
  • Appropriate zones, locations, and even clothing are marked with certain colours to achieve perfect segregation.
  • De-mineralization system and reverse osmosis (RO) water system at the Duo Pass Plant for Zero-Discharge Effluent Treatment
  • Administrative building with modern communication technologies, fully computerised individual/separate offices, and a server room. Adequate warehouse with distinct sections for packaging goods and raw materials.
  • For material management, we have provided centralized production planning software.

Quality Control and Quality Assurance 

Our quality control and quality assurance department has access to state-of-the-art analytical equipment. At all levels, all documented procedures are faithfully followed, and documentation including SOPs, calibration logs, and validation records are rigorously kept current. To improve our present formulae, streamline processes, and develop new products, we use a top-notch formulation and development lab.

A well-equipped lab with instruments like a UV-Vis spectrophotometer, Karl Fisher titrator, viscometer, and stability chambers is provided for in-house testing of all products. A location has been set aside for the microbiological lab.

Major Manufacturing, Quality Control, Utility Equipment

  • Ointment Mfg. Plant (500 kg)
  • Ointment Mfg. Plant (150 kg)
  • Tube Filling Machine 40 tubes/min
  • Liquid filling machine
  • Semi-solid (Lotion) filling machine
  • Labelling machine (Round and flat bottle)
  • Radhe Pharma
  • Analytical balance
  • RM sample weighing Balance
  • RLAF for Dispensing and Sampling 
  • Air Compressor 
  • HVAC system
  • Purified RO Water System with MB 250 lit/hr
  • Stability Chamber (1000 ltr) (3 nos.)
  • Viscometer 
  • UV-Vis Spectrophotometer
  • PH meter
  • Conductivity meter
  • Analytical Balance

Accreditation

Our manufacturing facilities are regularly accredited to follow rules and legislation. Our lab and manufacturing facilities are GMP Compliant, WHO GMP Certified, and D&B D-U-N-S Registered. Every single product created at AQMED Laboratories has received FDA of Gujarat approval.