Product development technology

PRODUCT DEVELOPMENT TECHNOLOGY CONTROLLED RELEASE PELLETS

STANDARD FEATURES :

Consists of Strip forming polymers, plasticizers, API, flavoring & coloring agent, etc.

Innovative, advanced IR & MR formulation & process technology.

The delivery of drug via film, in-process onset of action, tailored to meet your requirements.

Dedicated project management with method development and validation.

Enhance efficiency & safety profile of medicament.

Internal Technology transfer from laboratory to pilot plant to commercial technology.

Thin film is more stable, durable & quick dissolving than other forms.

Identifying the right key process parameters.

Thin film improves dose accuracy empowered to liquid / syrup dosage form.

Full scale production of at least three batches.

Ease of administration, beneficial for pediatric, geriatric & neurode generation disease.

Extended release (XR) or Long lasting (LA) allows for a decrease in dosing frequently.

Dissolving without made of water like patients with disorders / nausea.

SR- specific amount of drug release at time intervals.

Potential to develop sensitive drug targets.

Delayed or Enteric release formulation development is possible.

Sublingual film delivers a convenient, quick dissolving therapeutic dose.

API release at a specific point in body based on PH or other char. depending on drug profile.

Drug contained by film, rapidly absorbs under the tounge to ensure compliance.

Drug release in the intestine formulated to release at a higher PH (more basic)

From commercial prospective it offers extend revenue life cycle for drug patent expiring soon.

or drug release in stomach (more acidic).

Formulation development on a bench & pilot scale development.

Specific release pattern as per customer requirement can be developed.

Short term accelerated physical stability studies before a full scale development program.

Dossier preparation per product with scale up parameters for pilot and production scale.

Contract manufacturing for the products in our GMP approved facility.

Non-exclusive / exclusive arrangement to deliver treatments for your molecule.

Complete Technology transfer from product to pilot to large scale production possible.

GELATIN BEADS

HOT MELT EXTRUSION

STANDARD FEATURES :

Improves the bio availability of purely water soluble & purely permeable compounds.

Formulation development on bench scale.

Enhance dose uniformity of potent compounds and minimize variability.

Bench & pilot scale development for your products.

Reduce due time & benefit from a proven dosage form with stringent commercial success.

Enhance solubility, bio for purely soluble drugs.

Oil and pellets can be encapsulated by this technology.

Ability to incorporate taste masking.

Gelatin and other core pellets can be made as per project needs.

Broad selection of down stream process technology.

We work strictly under confidentiality agreements with customer defined time lines.

Granules for end in solid dosage form, incl. CR delivery formulations.

Formulation development on a bench & pilot scale development.

Heat sensitive molecules also can also be processed with special processing attachments.

Tailored to meet your product requirements.

Short term accelerated physical stability studies before a full scale development program.

A range of proto type formulations are prepared under different process conditions.

Analytical techniques applied as appropriate to determine formulation & process parameters.

Dossier preparation per product with scale up parameters for pilot and production scale.

Contract manufacturing for the products in our GMP approved facility.

Technology transfer with equipment purchase & support if needed.

Non-exclusive / exclusive arrangement to deliver treatments for your molecule.

Customer defined pellets can be made with customer ingredients / actives .

Hot melt pellets are also possible by attaching axillary equipments to the hot melt extruder.

Complete Technology transfer from product to pilot to large scale production possible.

Umang Pharmatech Pvt. Ltd. Survey No. 146, H. No.1 (PT), Vasai Phata Highway Junction, Pelhar, Nh8, Vasai (E) - 401 208, Maharashtra (India). Tel. : (+91-22) 30018900 / 30018915 - 98, Mob. : (+91) 986 723 6594, Fax : (+91-22) 30018908 / 30018913 E-mail : umang@umangpharmatech.com, Website : www.umangpharmatech.com / www.umangpharmaceuticals.com

www.umangphar maceuticals.com

MOUTH DISSOLVING FILM

PRODUCT DEVELOPMENT TECHNOLOGY MICRO PELLETS

STANDARD FEATURES :

Pulsed drug delivery is a mixture of different release pattern are mixed.

Micro pellets technology for 100 / 200 / 300 / 400 / 500 micron sizes.

Dedicated project management with method development and validation.

Internal Technology transfer from laboratory to pilot plant to commercial technology.

Identifying the right key process parameters.

Full scale production of at least three batches.

Controlled drug delivery of the products is possible with micro pellets.

Dedicated equipments for development.

Can be compressed into tablets.

Short term accelerated physical stability studies before a full scale development program.

Delayed or Enteric release formulation development is possible.

Dossier preparation per product with scale up parameters for pilot and production scale.

API release at a specific point in body based on PH or other char. depending on drug profile.

Contract manufacturing for the products in our GMP approved facility.

Micro pellets have a higher bulk density compared to API or granules.

Non-exclusive / exclusive arrangement to deliver treatments for your molecule.

Fill weight of the product is higher in the capsules due to smaller size.

Complete Technology transfer from product to pilot to large scale production possible.

Dedicated equipments for development.

Tailored to meet your product requirements.

Short term accelerated physical stability studies before a full scale development program.

A range of proto type formulations are prepared under different process conditions.

Dossier preparation per product with scale up parameters for pilot and production scale.

Analytical techniques applied as appropriate to determine formulation & process parameters.

Contract manufacturing for the products in our GMP approved facility. Non-exclusive / exclusive arrangement to deliver treatments for your molecule. Complete Technology transfer from product to pilot to large scale production possible.

BEADS IN BEAD TECHNOLOGY

MUPS TECHNOLOGY

STANDARD FEATURES :

Micro pellets technology for 100 / 200 / 300 / 400 / 500 micron sizes.

The pellets are being put into another large pellet size by a special process.

The pellets are being put into another large tablet.

This technology avoids interaction between molecules.