Excellence is an art won by training and habituation. We do not act rightly because we have virtue or excellence, but we rather have those because we have acted rightly. We are what we repeatedly do.
Excellence, then, is not an act but a habit.
- Aristotle
Maximaa Proyurveda produces premium quality Herbaceuticals and PhytoProbiotics. Good Manufacturing Practices (GMP) is rigorously followed in the manufacturing facility. The team continuously thrives to achieve and sustain the best quality practices.
The manufacturing facility is equipped with Automatic WHO-GMP Compliant machines for Syrup, Capsules, Powder, Oil and Gel. The Ultramodern Machines, Clean Room Environment and stringent quality norms (consistent QA /QC Checks) allow Maximaa Proyurveda to produce Herbaceuticals and PhytoProbiotics with uniform levels of batch-to-batch consistency and the customer gets the same premium quality product regardless of where it was purchased.
Maximaa Proyurveda has taken care of all aspects of the pharmaceutical industry:
- Personnel
- Premises
- Equipment
- Sanitation
- Documentation
- Production
- Quality Control
- Self-inspection
Personnel:
We believe that a company is a reflection of its people. We have a pool of exceedingly qualified and experienced top management with well trained and enthusiastic staff. The company provides equal opportunities to students stepping into the corporate world and help them develop into dynamic individuals. Timely training and knowledge assessment are the integral part of our yearly curriculum.
Training programs have been designed for all the employees for giving exposure in the following areas viz :
- Good Manufacturing Practices / Good Laboratory Practices
- Health & Hygiene
- Industrial Safety
- Functional Area Training is given on-job using Standard Operating Procedure (SOPs)
Premises:
The manufacturing Facilities are of adequate size and designed to meet unidirectional flow of material and segregated movement of people working in Production, Packaging and Maintenance in accordance to cGMP. All Manufacturing, Packaging, Storage and Holding areas are maintained in a clean and orderly fashion to minimize the possibility of error. All the surfaces of walls, ceiling and floor are of hard and impervious materials. The critical manufacturing areas are painted with epoxy resin material leading to total crevices free environment. The change rooms for workmen and supervisory staff are spacious and well ventilated with fresh filtered air. All the utility services are provided from the service floor avoiding any contamination and interference by maintenance activities. The premises are WHO GMP compliant and can pass any export related standards.
Critical Areas of our Manufacturing Facility:
- Capsule Department
- Liquid Department
- Powder Department
- Oil Department
- Gel Department
- Quality Control Department
- Quality Assurance Department
- RM Store
- Warehouse
Equipment:
Maximaa Proyurveda unit is equipped by fully automatic and semi-automatic machines complying with ICH and WHO standards. The premises are completely validated for all its components to assure high quality with consistency. All the production machineries are manufactured using GMP approved materials, mostly with Stainless Steel 314/316.
We have made it sure that the manufacturing operations are conducted in a safe and contamination free environment. Hence the manufacturing area is equipped by Laminar Air Flow System with HEPA filters ensuring a Clean Room Environment (Temperature, Humidity, Pressure, Bacteria, and Dust control) at all times
The Capsule Manufacturing area is maintained and operated in class 10,000 Clean Room Environment, provided with 90% recirculation air system with terminally placed HEPA filters which ensure that manufacturing is carried out in sterile zone which help us build the quality of product that we have committed to deliver to the society.
Sanitation:
Maximaa Proyurveda understands its accountabilities towards environment. Maximaa Proyurveda has both an ETP (Effluent Treatment Plant) and WTP (Water Treatment Plant) to conserve the environment.
Documentation:
SOPs are the core of any quality organization. The entire documentation system is well defined and regularly monitored. The required documents are prepared and checked by the concerned departments, authorized and distributed by the Quality Assurance Department.
Production:
The Entire operations are carried out under the supervision of expert technical staff. All the processing activities are recorded in the batch Production Records on the process proceeds. In process checks are carried out at predefined critical stages and the Q.A. department gives the final analysis once the batch rolls out and releases the complete evaluation of the batch document.
Quality Assurance and Quality Control:
Quality control and Quality Assurance department carries out the responsibility to review/issue important documents to assure the quality of the finished products. It carries out the function of approving or rejecting all procedure or specification impacting on identity, strength, quality & purity of the product. Some of the core functions of the department are validation of test methods, maintaining Records, evaluate, maintain & storage of reference standard for substances, monitor stability of products, participate in complaint investigation; participate in environmental monitoring, etc.
Self-inspection:
Self-inspection is encouraged in our system to ensure that we remain consistent with quality. Maximaa Proyurveda carries out this exercise twice a year involving quality experts from the industry.
Maximaa Proyurveda is the only Herbaceuticals Company to have Patented Herbal Range of Products in UNITED STATES, CHINA & INDIA.
Maximaa Proyurveda has not left a stone unturned in exploring the possibilities of combination of the ancient Ayurvedic science with the ideologies of modern science. It is due to such dedicated efforts that the novel progressive form of Ayurveda; PROYURVEDA was born.
Maximaa Proyurveda has a landmark laboratory equipped with most modern pharmaceutical instruments that facilitates continuous quality control, quality analysis, research and new formulation development. The laboratory is managed by a team of experienced doctors, scientists, chemists, PhDs, microbiologists and pharmacologists working under the GLP (Good Laboratory Practices) guidelines.
Laboratory Infrastructure:
- Formulation, Research & Development Unit
- Microbiology section
- Instrumentation section
- Analytical section
- Stability Chamber
- Control Centre Room
- Documentation Room
