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Analytical services - OEL: 50 ng/m3
Product Description
- Control of pharma samples solid state : Identification and quantification of solid state, method development and validation, routine QC.
- Analytical techniques available : XRPD, DSC, TGA, DVS, Laser PSD, FTIR, IDR.
- All analyses are applicable to toxic samples down to : 50 ng/m3.
- Various samples can be analyzed, from pure API to final formulation (e.g. powders, suspensions, tablets, ointments and more).
- A full detailed report is edited with relevant bibliographic search, comparisons and conclusions
Holodiag

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FR
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2015On CPHI since
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1 - 24Employees
Company types
Contract Research Organisation (CRO)
Primary activities
Analytical Services
Contract Research Organisation
Departments
General Management
Other
Categories
- Biopharmaceutical Products Analytical Chemistry (Biopharmaceutical Products)
- Biopharmaceutical Products Analytical Methods (Biopharmaceutical Products)
- Contract Development and Manufacturing Organisations (CDMOs) and Contract Manufacturing Organisations (CMOs) (Services) Analytical Development
- Contract Research Organisations (CROs) (Services) Contract Research
- Laboratory and Analytical Services (Services) Method Development
Holodiag

-
FR
-
2015On CPHI since
-
1 - 24Employees
Company types
Contract Research Organisation (CRO)
Primary activities
Analytical Services
Contract Research Organisation
Departments
General Management
Other
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• These studies bring together knowledge on the nature of the solid states of a given compound (intermediates or APIs) and its associated properties (stability, solubility, dissolution) in order to select the right solid phase. • Screening operated: salts, cocrystals, polymorphs and amorphous solid dispe...
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Physico-Chemical testing
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Product Sterile Sodium Hyaluronate (Hyaluronic Acid)
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Product Drug Stability Testing and ICH Storage Outsourcing
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Product PHARMACEUTICAL ANALYSIS DEPARTMENT
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Product R&D service
Neotron Pharma is able to offer you a research and development service. The research and development laboratory, operating under the ISO regime, will be able to develop customized methods for the customer in faster times and with lower costs. Subsequently, the customer will be able to validate the GMP meth... -
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