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NBC Pharma Solutions

Training Duration : 20 Working DaysTheory Hours : 20 HoursTheory with online Practical Hours : 40 HoursMaximum Class Size : 20 Members

Reach us:

KNBC PHARMA SOLUTIONS PVT. LTD.3rd Floor, Plot No. 177, I. D. A. Mallapur

Hyderabad - 500 076, Andhra Pradesh, India.

Reach us:

3rd Floor, Plot No. 177, I. D. A. MallapurHyderabad - 500 076, Andhra Pradesh, India.

KNBC PHARMA SOLUTIONS PVT. LTD.

We are specially designed 100% certified job oriented

"HANDS ON TRAINING" programme for Science

and Pharmacy Graduates and jobseekers on

“PHARMACEUTICAL ANALYSIS TRAINING”. The

course covers various testing procedures adopted in

Pharmaceutical Industries (Bulk Drugs and

Formulations). Practical Training will be provided on

latest Instruments. The training also covers the

Topics on facing Interview, personality development,

Quality Control and Analytical Development. We also

impart training to individuals to suite their needs as

per their requirement.

LC MS/MS Operation, Calibration & Troubleshooting

HPLC Operation, Calibration and Trouble Shooting

GC Operation, Calibration and Trouble Shooting

FTIR Operation, Calibration and Trouble Shooting

Dissolution Tester Operation, Calibration and

Trouble Shooting

Disintegration Tester Operation and Calibration

Volumetric Solutions Preparation and

Standardization

Friability Tester Operation and Calibration

Limit Test Analysis (Sulphates, Chlorides and etc)

TLC Techniques

All types of Instrumental Analysis of Tablets,

Injectables and Bulk drugs

All types of Chemical Analysis of Tablets,

Injectables and Bulk drugs

TRAINING TOPICS

(THEORY WITH PRACTICALS)

TRAINING TOPICS

(THEORY WITH PRACTICALS)

ABOUT USABOUT US

SERVICESSERVICES

KNBC pharma solutions is testing laboratory equipped

with Highly qualified and well experienced scientific team

Strict adherence to its core values of ethics, safety and

reliability in supporting to work for customers. Imparting

best analytical services to various clients who are into

manufacturing of Bulk drugs, Api's, Formulation, research

and development and government agencies.

Analytical Services

Synthetic Services

Auditing Services

Guidelines Followed:

·

· Analytical method validations

· Estimation of Genotoxic impurities

· Answering Rugulatory / Agency queries

· Isolation of process related impurities by

Preparative

· Preparation of Intermediates

· Synthesizing of process related impurities.

· Optimizing the Cost effective Synthetic

schemes

Independent quality assurance team

· Performing Study based audits

· Performing process based audits

· Performing Facility based audits

· Performing quality based audits

Indian pharmacopia(IP)

British pharmacopia (BP)

United states pharmacopia (USP)

Europian pharmacopia (EP)

ICH guidelines

Analytical Method development

·

1. IMPURITY ISOLATION

2. IMPURITY SYNTHESIS

3. CERTIFIED IMPURITY STANDARDS

4. COST EFFECTIVE SCIENTIFIC SOLUTION

5. LYOPHILIZATION SERVICES

6. OTHER USER SPECIFIC SUPPORT

7. STRUCTURE INTERPRETATION

Isolation and purification of impurity from mg to g scale. We have executed most critical isolation and purification project in recent past, e.g isolation of unknown impurity from drug product and APIs and and Structure elucidation.

We have synthesized impurities as on date. We offer custom synthesis of impurity compounds on requests. For a quote on this service please submit the following information:

A) Structure of the impurity. B) Name of the parent compound. C) Required quantity.

All products are supplied with certificates of analysis. Standard certificates contain:

A) Identification by 1H-NMR and Mass spectroscopy. B) Purity test by either HPLC or GC. C) Other test like C13-NMR, TGA, IR & Elemental Analysis will be provide on request.

We are manufacturing impurity in gm level. Our prices are lowest prices in the world.

We are providing this typical service, all kinds of sample which are very sensitive to temperature.We have Virtis 25EL, Capacity of freeze drying is 500 g/day.

We are supporting our client for analytical method development, formulation development, in-vitro-invivo studies, preformation studies, impurity profiling, leaching study, tech-tanfer issues and FDA query response.

Study of spatial heterogeneity of reactants, products, or conditions by using 2-D NMR techniques involving Homonuclear correlation experiments like NOESY, DQF-COSY, TOCSY, ROESY and Heteronuclear correlation experiments like HMQC, HSQC, HMBC.Quantification studies by NMR. MS/MS studies and mass accuracy up to 4th decimal - Q-TOF. For volatile / neutral molecules with less than 500 amu GCMS,

t Screening of Genotoxic Impurities

t Evaluation & Estimation of Genotoxic

Impurities & Method Validation

t Analytical Method Validation of

Pharmacopoeial Methods

t Analytical Method Validation of

Related Substances (Impurity Profile)

t Analytical Method Validation of

Residual solvents in ppm levels

t Analytical Method Validation of Assay

(Chromatographic and potentiometric)

t Analytical Cleaning Method Validation

of Rinsing and Swab method

t Analytical Method Validation of Chiral

Method by HPLC

t Injectables, Syrups, Ointments

t Formulation Tablets, Capsules

t Excipients

t Raw Materials

t Intermediates and In-process

Samples

t Identification by IR, UV, HPLC, GC, MR

t Related Substances by HPLC, GC

t Assay by HPLC, GC, UV, Potentiometer

t Residual Solvents by Headspace

method and Liquid method

t Loss on Drying

t Limit Tests for Metals (As per

Pharmacopoeia method)

t Residue on Ignition Solubility test

t Melting Point and Range

OUR STRENGTHOUR STRENGTH