Pharmaceutical Analysis
Services Pharmaceutical Analysis
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Catering to the Pharmaceutical Industry, our quality testing services has been valuable for examining the effectiveness of our drugs and medicines. The services of Applied Pharmaceutical Analysis rendered by us analyze pharmaceuticals on different parameters like bio analysis, impurity detection, In-Vitro Equivalence, Method Validation, DMF, CTD-Analytical Support etc. All these testing and analysis are done in our advanced laboratory by the team of experts. Besides, we offer our pharmaceutical testing services at the very affordable rates as against the orderly laboratories. Apart from that, we are considered as one of the most trusted laboratories offering Pharmaceutical Analysis Services in India.
Pharma Analysis
- Raw Materials as per IP/BP/USP/or any other specification excluding analysis on instruments.
- Any single test as per IP not requiring, use of analysis on instruments Finished product by chemical analysis.
- Single product by chemical analysis (Assay by chemical method).
- Additional ingredients (other than vitamins).
- Tablets /capsules / dry syrups /suspension / injections /ampoule (Physical parameters).
- Vitamins 1st ingredient (Except micro)
Additional each ingredient (except micro). - Uniformity of content(chemical)
- Uniformity of content (UV)
- Uniformity of content (HPLC isocratic)
- Uniformity of content (HPLC gradient)
- Vitamin A assay (chemical)
- Vitamin D assay by HPLC
- Folic acid assay
Water for injection IP Analysis using sophisticated instruments - Thin layer chromatography, qualitative, each run.
- Thin layer chromatography using costly impurities, qualitative, each run
- UV Spectrophotometer Analysis
- UV Spectrophotometer Analysis (using organic solvent as medium)
- Dissolution test using UV.(as per IP /BP/ USP)
- Dissolution test using UV.(as per IP /BP/ USP) 3 Time points
- Dissolution test using HPLC(Isocratic)(as per IP /BP/ USP)
- Dissolution test using HPLC.( Isocratic )(as per IP /BP/ USP) 3 Time points
- Dissolution test using HPLC.(Gradient) (as per IP /BP/ USP)
- Dissolution test using HPLC.(Gradient) (as per IP /BP/ USP) 3 Time points
- Raw material &Finished product using HPLC (isocratic reverse phase)
- Raw material &Finished product using HPLC (gradient reverse phase)
- Raw material & Finished product using HPLC (isocratic normal phase)
- Raw material &Finished product using HPLC (gradient normal phase)
- Uniformity of content using HPLC
- Related substances using HPLC (each run)
- Vitamin A, D3 using HPLC (in combination) Gas chromatography
- Raw material (each run)
- Finished product (each run)
- Organic volatile impurities (each run)
- Head space sample injector on capillary column (each run)
- Organic solvent each run (pack)
- Atomic absorption spectrophometer (per element)
- Consistency
- Acid value, hydroxyl value, saponification value, acetyl value, iodine value (each)
- Paper chromatography (each)
- Column chromatography (each)
- Water by Karl Fischer
ISL will conduct analysis according to IP/ BP/ USP/ EP/ IS/AOAC/APHA or as per party specification and the same will be mentioned on the report.Party to submit sealed samples in duplicate for analysis.Service tax will be charged extra.Charges will vary from product to product.
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ISL will conduct analysis according to IP/ BP/ USP/ EP/ IS/AOAC/APHA or as per party specification and the same will be mentioned on the report.
Party to submit sealed samples in duplicate for analysis.
Service tax will be charged extra.
Charges will vary from product to product.
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SERVICES
