Anhydrous Ethanol / Pharmaceutical Quality
Absolute Alcohol min. 99.9% vol.
(Item No: PH.EUR.520MT2) in accordance with the European Pharmacopoeia
Currenty only on request
Active pharmaceutical (API) ingredient and exipient for pharmaceutical use
Azeotropic Ethanol / Pharmaceutical Quality
Ethanol (Pharmaceutical) min. 96.0% vol.
(Item No: PH.EUR.450MT2) in accordance with the European Pharmacopoeia
Active pharmaceutical (API) ingredient and exipient for pharmaceutical use
Denaturation
Standard Denaturation (per 100 Liters of pure Alcohol):
- min. 1 Liter Methyl ethyl ketone (MEK- denaturant)
- min. 1 Liter pure Methyl ethyl ketone (2 Butanone)
Information
Certified GMP Pharmaceutical Manufacturer
- Manufacturing license according to § 13, Paragraph 1 of the AMG (German Drug Law)
- Certified GMP pharmaceutical manufacturer according to Article 111 (5), Directive 2001/83/EG
Continuous production monitoring through internal monitoring processes
- Analysis of pre-finished and finished products in our own laboratory
- Continuous certification of suppliers and service providers
- GMP-compliant batch release in accordance with the current version of the European Pharmacopoeia by a qualified person
Delivery to well-known pharmaceutical companies at home and abroad
- Use of ethanol as active ingredient and excipient
- Regular audits by pharmaceutical manufacturers
Storage and logistics of pharmaceutical ethanol
- Separate tanks for the storage of the pharmaceutical ethanol qualities
- Separate pipelines for storage and retrieval
- Hermetically sealed product handling
- GMP-compliant transport through qualified logistics partners
- Computer-controlled online denaturing