Your project: Analysis of starting materials
Your time-line: as soon as possible
Procedure: European Pharmacopoeia (Ph. Eur.),
US Pharmacopoeia (USP), your methods
Our offer: Testing of starting materials according to European Pharmacopoeia (Ph. Eur.), US Pharmacopoeia (USP), customer specific methods, complete testing as well as analysis of individual parameters
Methodology: European Pharmacopoeia (Ph. Eur.)
US Pharmacopoeia (USP)
Customer specific methods
Our competence: Experience in testing of a lot of different active ingredients and additives.

Special determinations such as:
Flowability, Ph. Eur. 2.9.16
Apparent volume, Ph. Eur. 2.9.15
Consistency by penetrometry, Ph. Eur. 2.9.9
Sieve analysis, Ph. Eur. 2.9.12 and 2.9.38
Nephelometry, Ph. Eur. 2.2.1
Viskosity, Ph. Eur. and USP
IR-/NIR-spectrophotometry
light microscopy
particle size distribution by means of laser diffraction
HPLC with refractive index detection, fluorescence detection, evaporative light-scattering detection
densitometry, fluorimetry, photometry

Working on highly potent substances such as cytotoxics, hormones, antibiotics, narcotics

Examination of primary containers, closure systems, foils and secondary packaging systems

We deliver suitable sampling bottles to you

Short-term processing of your orders

Please contact: Steffen Durst, Ph.D., Biologist
Fon: 0049 (0)7251 72484-05
Fax 0049 (0)7251 72484-29
info(Replace this parenthesis with the @ sign)techpharm.de

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