Company Profile

History of Formation :
Nivon Specialties was founded in the year 1999 by professionally driven individual who has more than 16 years experience in pharmaceutical field.
We at Nivon Specialties believe that service, excellent quality, timely delivery and competitive rates are our forte.

Profile :
Nivon Specialties is indulged in Contract manufacturing and Export of Pharmaceutical Products both in Active Pharmaceutical Ingredients API's and Formulations in various dosage forms ( Tablets, Capsules, Syrups, Injections, Metered Dose Inhalers) upto advanced drug intermediates.
The Company covers a long range of Products & activities guided by the marketing team having expertise in their respective fields.
Pharmaceutical Dosage Formulations are being manufactured under strict vigilance at sites approved vide WHO-GMP Standards.
The Company has its Head Office at Vashi, Navi Mumbai one of the fastest growing twin commercial capital of India.

Mission :
“To become an integrated, customer centric company with a global footprint.”

Quality Policy :
Quality is the soul of our products. Purity of soul depicts the very essence of a product. Our quality policy is the guiding light to the maintenance of quality throughout the shelf life of our products.

Vision :
We contemplate ourselves to be the front-runner in the march toward achieving undisputed leadership in the field of choice by a proven ability in high quality efficiency and in the undoubted trust by our clients. We believe in healthy competition as it offers us an opportunity to demonstrate our superiority and encourages us to take on the challenge to gallop ahead to shape the future in the right direction.

Management :
The Company's management is dynamic in marketing & technical fields and is sensitive to changing customer requirement. The Company has a team of highly qualified and professionals who are committed to excellence in terms of product quality, productivity, cost-efficiency and delivery.

Manufacturing Facility :
The Company gets its entire products manufactured under contract manufacturing from WHO-GMP certified units under the able supervision of our team of experts. we give clear preference to best quality ingredients to produce finest finish of products stable throughout their shelf life.

Quality Control :
In order to achieve the highest quality product the manufacturing facilities are ably supported by in-process testing laboratory fully equipped with the latest equipment like GC , HPLC ,I.R, Spectrophotometers and Microbiology department to monitor the quality of the products. The quality assurance section works to stringent ISO-9001-2000 guidelines besides helping other departments to ensure implementation of the ISO quality system in every activity.

Global Presence :
Nivon Specialties is a 100 % Export Oriented Company . Several foreign countries are already on the cards including Guatemala, Iran, Panama, Philippines, China, USA, Canada, Central African Republic.

Customer Care :
A Customer to us is the most important visitor. He is the one who brings us business; the one who plays a key role in our progress towards prosperity and growth; the one whose acceptance enhances our glory and non-acceptance our doom. We exist in the market because of his gratitude. We rule the roost because of his ironclad support. The Customer Care is therefore a solitary and mandatory obligation for us.

Quality Assurance :
Nivon Specialties is committed to total quality management. Our associates manufacturing process is carried out under strict supervision of technically competent staff as per the pre-defined processes and procedures. To ensure that the cGMP standards are met and products comply with international quality standards; quality control measures have been imbibed at various stages of production starting from approval of raw materials, in-process materials and extends to checking of finished products. The Batch Manufacturing Records and Batch Packaging Records are maintained for all manufactured products. The Final products are tested to the strictest of the available international pharmacopeial standards and norms. Stability studies are conducted on all our manufactured products.

Regulatory compliance :
We ensure that implementation of cGMP standards are followed by the technical packages comprising of Drug Master files, Product Dossiers, Free sale certificates, Certificate of Pharmaceutical Products, etc.