We take this opportunity to emphasize that now we are accelerating more steps towards QUALITY ASSURANCE. We have now a dedicated R&D team putting their energy and concentration into sustainable improvement in products, packing, design, and quality. Presently we are having our own WHO/GMP unit HABITARE PHARMA PVT LTD under Non-Beta 4 sections Tablet, Capsule, Ointment & Syrups. Along with that, we are incorporated with WHO-GMP manufacturing units for the production of other products but now we are happy to Onboard leading EU-GMP Manufacturing Plants that are exporting Goods to Leading MNC Companies.
We never compromise on the basis of quality. We not only say by mouth, but all the products which we send are also going through a testing process. If they pass then only we sell to our distribution partners, else even a dilution problem sends back the whole stock. We provide testing reports of each batch we are selling in the market. So, WE NEVER COMPROMISE ON THE BASIS OF QUALITY
By entering the pharmaceutical industry, BIOFIELD Pharma Pvt Ltd made every effort to fulfill its mission of assisting the Nation. Increasing capacity utilization, creating pharmaceutical items of the highest caliber, improving the product, or delivering it at the proper place and time are just a few examples. To continuously improve pharmaceutical products for patients, the company leverages cutting-edge technologies. At Quality Innovations, we put a lot of effort into enhancing human life quality and have a passionate, distinct vision for the future. The business of BIOFIELD Pharma Pvt Ltd is conducted in conformity & compliance with applicable quality regulations, codes, and standards. Records, documentation, and data are managed by applicable regulations. We provide a wide range of around 950+ products in the categories of GENERAL, GYNAE, ORTHO, PEDIA, DERMA, PAIN MANAGEMENT, CARDIAC & DIABETIC, UNIQUE MOLECULES which include antibiotics and anti-infectives, multivitamins and minerals, anti-allergic, antioxidants, painkillers, hormonal management and a lot more. All our products are available in capsules, tablets, liquid, gel capsules, dry powder, ointment, etc.
The pharmaceutical quality system (PQS) aims for continuous development. BIOFIELD Pharma is an ISO 9001-2008 ICH Q10 standards, WHO, GMP Certified Pharma Franchise organization that also conducts business in India. Our organization's dedication to improvement is addressed in our quality policy. It is not necessary to describe the CAPA or management review processes or other continuous improvement strategies. It should instead make a quick mention of improvement. We are having our own WHO/GMP manufacturing unit for Tablets, capsules, Ointments, and syrups. We have NON-BETA Manufacturing Plant. Any 3rd party products or brands you are working on, you are more than welcome to start working with us with Competitive rates and the best quality. BIOFIELD Pharma Pvt Ltd continuously reviews its various operations to make them more efficient, and relevant to changing international scenarios. We stringently adhere to implementing Quality Management Systems and are committed to making continual improvements to the same.
A quality policy, which explains the "why" behind this strategy, is a cultural cornerstone of BIOFIELD Pharma Pvt Ltd. Patient safety is the moral thing to do, hence quality and ethics are strongly related in the pharmaceutical industry. Our policy briefly discusses cultural ideals of integrity and other moral principles. As a key component of our company's purpose and mission, BIOFIELD Pharma Pvt Ltd is dedicated to providing patients and consumers with safe and efficient products.
To meet this commitment, BIOFIELD Pharma Pvt Ltd maintains a quality-focused culture to ensure the highest priority is placed on the safety, efficacy, and reliability of our products, the safety of our patients and consumers, the quality of data supporting regulatory submissions, and interactions with our stakeholders. To promote quality-focused behaviors and guarantee that decisions are made in the best interests of product quality, patient and customer safety, and the preservation of BIOFIELD Pharma Pvt Ltd.'s brand and operations, the company is committed to upholding a culture of quality.
QUALITY POLICY:
As part of a long-term, morally-binding policy, BIOFIELD targets and commits to selling only goods that adhere to cGMP requirements. By providing pharma products that adhere to a variety of quality standards and arrive on schedule, we consistently work to satisfy our customers. We consider the viewpoint of the customer and provide them with timely access to all necessary technical facts and information. We regularly assess all of our activities to improve their effectiveness, global context relevance, and environmental friendliness. We abide by all pertinent legal and administrative obligations. Providing training to our staff is a regular event on our calendar that promotes teamwork and informs them of the latest developments and accomplishments in the business globally.
QUALITY ASSURANCE:
The development team's unwavering motivation and passion are focused solely on making sure that our manufactured products are of the highest quality to achieve optimum efficacy.
GOOD MANUFACTURING PRACTICE (GMP):
ensures that products are consistently produced and controlled in compliance with quality standards in place, appropriate for their intended use; supplying our cherished consumers with the greatest products and services possible; diligent oversight of our operations following numerous regulatory standards and ongoing development supported by intensive research initiatives; fostering an awareness of health, safety, and the environment by planning frequent training sessions and other initiatives to meet social obligations and make the BDR environment an ideal and desired workplace. monitoring multiple systems around-the-clock to guarantee stringent and unwavering adherence to product quality standards
QUALITY CONTROL:
The Quality Control (QC) division is well-equipped with contemporary tools and methods to conduct microbiological analysis as well as analyses of raw materials, packing materials, and intermediate and finished medicinal ingredients. The analysis of the goods produced on the premises is done by approved requirements. Every manufactured and supplied piece of packaging and raw material is analyzed by predetermined guidelines. Chemical and microbiological testing is regularly used to check the quality of water, and the Engineering, Quality Assurance, and Production departments receive regular feedback to take any necessary corrective actions.
Only after conducting all necessary analyses and determining that the raw materials, in-process materials, and packing materials are sufficiently satisfactory are, they approved for release by quality control (QC). Procedures are also defined for environmental monitoring, which includes routine microbiological monitoring of the air, surfaces, and workers in the production area. Examinations for the total viable count and the absence of pathogens are part of microbiological analysis. Specifications, standard test methods (Method of Analysis), and acceptance criteria
are well documented and revised by the Quality Control department from time to time. These documents are approved and controlled by the Quality Assurance department. The Quality Assurance department reviews and approves all Standard Operating Procedures before implementation. All the activities in Quality Control are carried out as per laid down Standard Operating Procedures. Each person in BIOFIELD is accountable for ensuring product quality, and patient and consumer safety. Division leaders are accountable to ensure procedures are in place that adequately defines the expectations for work that supports, or directly affect, product quality, product registration, and/or data that support product quality and patient or consumer safety; All Colleagues and Contingent Workers have the appropriate education, training, skills, and experience to carry out their work competently, by applicable regulations and Pfizer policies and procedures; Records, documentation, and data are managed by applicable regulations.
