We accelerate Research and Development activities for our partners by offering formulation development services at cost effective solutions. We provide development services for different dosage forms such as Oral Solids, Injectables, Oral Liquids and Topicals.
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Active Pharmaceutical Ingredients Sourcing and qualification
Inactive Pharmaceutical Ingredients/Excipients, Packing Materials Sourcing and qualification
Pre-formulation Studies
Product Development through QbD approach
Prototype Development
CMAs, CQA and CPPs are identified through DoE
Formulation development of products that require Low Relative Humidity (<30%)
Packaging Development
Optimizing the existing formulation and analytical methods.
Analytical Method Development and Validation
Reverse Engineering Of Reference Product
Technology transfer of product to partner’s preferred manufacturer
Clinical CRO Coordination: Axxelent can coordinate with Clinical CROs to qualify and executing the Pilot/Pivotal BE studies.
Axxelent can provide its expertise to all Technology Transfer and troubleshooting projects at validation levels.
Preclinical and Clinical Phase Product Development for NCEs.
Film-coated tablets are conventional tablets coated with a thin layer of polymer.Sugar coated tablets are compressed tablets that have been coated with concentrated sugar solution.
ODT differ from traditional tablets in that they are designed to be dissolved on the tongue rather than swallowed whole.
Chewable tablets are tablets which are difficult to swallow and thus, are chewed within the buccal cavity prior to swallowing.
Sublingual tablets are tablets that are intended to be dissolved beneath the tongue for absorption through the oral mucosa to produce a systemic effect.
A bilayer tablet involves the compression of two formulations into a single solid oral tablet, while maintaining a physical separation of the formulations by layering one on top of the other.
Dosage form where in which the drug is encapsulated inside the capsule shells.
Matrix tablets are the type of controlled drug delivery systems, which release the drug in continuous manner. In a matrix system, the drug substance is homogenously mixed into the rate controlling material as crystalline, amorphous or in rare cases molecular dispersion.
These are Matrix type dosage forms wherein which the matrices are prepared by Lipid Waxes and related substacnes.
Dosage forms that releases the drug only at some point after the initial administration.
A bilayer tablet involves the compression of two formulations of Immediate release and Modified release into a single solid oral tablet.
These are pellets which are spherical, free flowing granules with Narrow size range, coated with Delayed release polymer.
MUPS is a multiparticulate pharmaceutical solid dosage form produced by compressing a mixture of drug-containing pellets and powder excipients.
A suspension is a heterogeneous mixture in which the solute particles do not dissolve, but get suspended throughout the bulk of the solvent, left floating around freely in the medium.
Homogeneous liquid preparations that contain one or more chemical substances dissolved, i.e., molecularly dispersed, in a suitable solvent or mixture of mutually miscible solvents.
Dosage forms which contains freeze dried powder of the product which are reconsituted before adminstration.
Dosage forms which contains the drug in the liquid forms.
A pre-filled syringe is a disposable syringe that is supplied already loaded with the substance to be injected.
A hermetically sealed small bulbous glass vessel that is used to hold a Sterile Medical solution for subcutaneous, intramuscular, or intravenous injection.
Gels are semisolid systems in which there is interaction between colloidal particles within a liquid vehicle.
Creams are semisolid dosage forms containing water or volatile components and typically less than 50% hydrocarbons, waxes, or polyols as vehicles. They may also contain one or more drug substances dissolved or dispersed in a suitable cream base.
Pastes are the semisolid preparations intended for external application to the skin. Usually they are thick and do not melt at normal temperature.
Lotions are usually liquid suspensions or dispersions intended for external application to the body.
Film-coated tablets are conventional tablets coated with a thin layer of polymer.Sugar coated tablets are compressed tablets that have been coated with concentrated sugar solution.
ODT differ from traditional tablets in that they are designed to be dissolved on the tongue rather than swallowed whole.
Chewable tablets are tablets which are difficult to swallow and thus, are chewed within the buccal cavity prior to swallowing.
Sublingual tablets are tablets that are intended to be dissolved beneath the tongue for absorption through the oral mucosa to produce a systemic effect.
A bilayer tablet involves the compression of two formulations into a single solid oral tablet, while maintaining a physical separation of the formulations by layering one on top of the other.
Dosage form where in which the drug is encapsulated inside the capsule shells.
Matrix tablets are the type of controlled drug delivery systems, which release the drug in continuous manner. In a matrix system, the drug substance is homogenously mixed into the rate controlling material as crystalline, amorphous or in rare cases molecular dispersion.
These are Matrix type dosage forms wherein which the matrices are prepared by Lipid Waxes and related substacnes.
Dosage forms that releases the drug only at some point after the initial administration.
A bilayer tablet involves the compression of two formulations of Immediate release and Modified release into a single solid oral tablet.
These are pellets which are spherical, free flowing granules with Narrow size range, coated with Delayed release polymer.
A suspension is a heterogeneous mixture in which the solute particles do not dissolve, but get suspended throughout the bulk of the solvent, left floating around freely in the medium.
Homogeneous liquid preparations that contain one or more chemical substances dissolved, i.e., molecularly dispersed, in a suitable solvent or mixture of mutually miscible solvents.
Dosage forms which contains freeze dried powder of the product which are reconsituted before adminstration.
Dosage forms which contains the drug in the liquid forms.
A pre-filled syringe is a disposable syringe that is supplied already loaded with the substance to be injected.
A hermetically sealed small bulbous glass vessel that is used to hold a Sterile Medical solution for subcutaneous, intramuscular, or intravenous injection.
Gels are semisolid systems in which there is interaction between colloidal particles within a liquid vehicle.
Creams are semisolid dosage forms containing water or volatile components and typically less than 50% hydrocarbons, waxes, or polyols as vehicles. They may also contain one or more drug substances dissolved or dispersed in a suitable cream base.
Pastes are the semisolid preparations intended for external application to the skin. Usually they are thick and do not melt at normal temperature.
Lotions are usually liquid suspensions or dispersions intended for external application to the body.
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Headquartered in Chennai, India, Axxelent is focused on Contract Development of Oral Solid Dosage, Injectables, Ophthalmic, Oral Liquids and Topicals and Manufacturing of Oral Solid Dosage, Oral Liquids and Topicals (Block-1) and Injectables & Ophthalmic (Block-2), for markets across the world including Europe and North America.
CIN : U24110TN2019PTC131943
Axxelent Pharma Science Pvt. Ltd., Module No.1, 10th Floor
A Block, IIT Madras Research Park, Kanagam Road, Taramani, Chennai-600113.
Tamil Nadu, India.
Call Us On : +91-44-61727900
Email Us : info@axxelent.com
SEZ UNIT No.910, Portia Road, Sri City, Tirupati District,
Andhra Pradesh, 517646.
Andhra Pradesh, India.
Call Us On : +91 8576 691100
Email Us : info@axxelent.com
3 Jagadeeswaran Street
T.Nagar
Chennai-600017, India.
Call Us On : 044-69127900
Email Us : info@axxelent.com
Expansion of Phase 2 Manufacturing for Small Volume Parenteral“Axxelent R&D unit received Recognition letter & Registration Certificate from DSIR, Ministry of Science and Technology, Govt. of India”