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发布时间: 2023 - 06 - 13
The roots of DFE Pharma date back to more than 100 years ago, when two dairy producers, in both the Netherlands and New Zealand, gradually transformed into modern producers of lactose excipients and joined to become the world’s leading excipient manufacturer. The abbreviation of these two companies DMV-Fonterra Excipients, led to the first part of our name, “DFE”, which is complemented by “Pharma”, as we are an independent company focused on the (bio)pharmaceutical and nutraceutical industry, by providing a broad premium quality portfolio of excipients for use in Biopharma, Inhalation, Oral Solid Dose and Nutraceuticals products.Since 2020, DFE Pharma is jointly owned by Royal FrieslandCampina, one of the world’s top multi-national dairy companies, and CVC Capital Partners, a leading globa...
发布时间: 2019 - 11 - 14
SIO HistorySIO’s beginnings date back to 1907, and today, is one of the most important global pharmaceutical oil manufacturer.As a subsidiary of Archer Daniels Midland Company since 1996, our company manufactures state-of-the-art purified pharmaceutical oils that can be used as APIs or as excipients for oral, topical and injectable formulations of oil-soluble drugs. With more than a century of experience in the manufacture of specialty oils, we also offer the best ingredients of vegetable origin for various applications in human and animal nutrition (e.g. hydrogenated vegetable oils for encapsulation) and cosmetic industries (e.g. high melting point vegetable oils and butters).On the below historical timeline, you have an overview on the major steps that made ADM-SIO become a key player in...
发布时间: 2017 - 07 - 05
CP Kelco, a Huber company, is an innovation leader in the production of polysaccharides by microbial fermentation, extraction from land and sea plants and modification of cellulose based raw materials. With over 200 years of experience, they are experts in hydrocolloid manufacturing, modification and application.Through the use of nature based chemistry, CP Kelco strives to provide products such as Xanthan Gum, Gellan Gum and Carboxymethylcellulose Sodium with minimal modifications. These hydrocolloids in turn serve multiple functions such as viscosity modification, thickening agent, suspension stabilization and gelation.With operations in several diverse global markets and a focus on responsible business practices, environmental stewardship and ethical conduct, the company has reached gre...
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Quality Chemicals

Quality Chemicals

上市日期: 2020-02-20

Country of Origin: Spain

Magnesium Hydroxide

Sodium Selenite Pentahydrate

Calcium Acetate

Quality Chemicals is a European manufacturer of high-purity salts. We are a chemical science company bringing raw materials to all kind of industries: pharma, biopharmaceuticals, veterinary, nutrition, nutraceuticals, personal care and oral care, industrial, laboratory reagents, etc.

We have been in the market for more than 70 years. Some of our current shareholders have been in the company for more than 40 years. Quality Chemicals is an independent company which allows us to focus on long-term goals that guarantee stability for both our customers and our team.

The company was initially based in Badalona, a town adjoining Barcelona, but in 2000 we moved to our facilities in Esparreguera, 30 minutes away from Barcelona and where our headquarters is located.

We have two production plants, one in Esparreguera and another in Venta de Baños, Palencia.  Over the last 5 years we have invested mainly in our GMP production facilities where we have great growth potential. We have more than 25 APIs registered and every year we develop 5 new APIs on average.

We have over 80 employees and a worldwide presence mainly in Europe and the US.

Our passion and vocation is chemistry. We are driven by this passion to explore the magnificence of this science and turn it into a way of making our customers’lives easier.

For more information, please visit:  https://www.qualitychemicals.com/

Quality Chemicals

Quality Chemicals

Quality Chemicals


Quality Chemicals’ facilities are designed essentially for the following purposes:

Chemical synthesis, especially of inorganic products.

Distilling a great variety of chemical products.

Process control and analysis.

Our production facilities feature:

Versatility, which allows us to manufacture many different types of products (multi-purpose plant).

* Different reaction capacities (from kilos to tonnes).

* Target products: salts, acids, solvents, synthesis intermediates, ready-to-use products, etc.

* Equipment: stainless and enamelled reactors, distillation columns, dryers and all the tools suited

to specific needs.

* Quality management based on fulfilment of SOPs (Standard Operating Procedures). This system

ensures the traceability of the product throughout the manufacturing process.

GMP Plant

This plant has been operating since 2004 and complies with GMP guidelines ICH-Q7 – EU-GMP part II.

It mainly produces excipients and API for the pharma, veterinary and biopharmaceuticals industries.

However, it also manufactures nitrates, acetates, phosphates and sulphates for other industrial 

applications such as foodstuffs and personal care.

In 2015 we earned Spanish Agency of Medicines and Medical Devices authorisation to produce API.

We can supply any of our products manufactured under GMP conditions.

These GMP products are usually used by pharmaceutical, biopharmaceutical

and veterinary companies and can be used as:

• Reagents

• Starting material

• Excipients


They are produced under the European GMP Guide for the manufacturing of drug products part II,

active substances (ICH Q7). We also offer multicompedial products: the product can be supplied 

in compliance with the quality standards of individual pharmacopoeias, a combination of several of

them or even without a monograph in any pharmacopoeia.

With our GMP grade you get the following benefits:

• Fast track to market, fast registration

• High quality and safe raw materials; easier and safer to get process approval

• Dossiers ready-to-use, no need to develop test methods or evaluate stability data

• Compliance with international regulatory standards

With the GMP grade we offer:

• Strict working conditions following ICH guideline Q7-part II

• Customised solutions and tailored packaging to meet your needs

• Change control

• Full traceability

• Supplier audits

• Dedicated regulatory support

• Comprehensive dossiers in the international CTD format, acc. to ICH Module 3.

Please find more details about documents at  “Supporting Documents” at Support in the Menu.

We have been regularly inspected by the Spanish Agency of Medicines and Medical Devices

(AEMPS) since 2015, which means our quality assurance system is regularly monitored and

audited by this authority. Our quality system is also monitored by 30 audits per year by our pharma,

cosmetics and food industry customers.

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