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Dissolution Apparatus Manufacturer India – Scientico

Scientico manufactures Dissolution Apparatus (Dissolution Testing Machine) for pharmacy college laboratories. Our dissolution apparatus is ISO 9001:2015 and model-specific and complies with USP and IP pharmacopoeial standards, making it suitable for B.Pharm, M.Pharm, and D.Pharm labs under Pharmacy Council of India (PCI) regulations.

Types Available

  • USP Type I, Rotating Basket (6 and 8 vessel)
  • USP Type II, Paddle Apparatus (6 and 8 vessel)
  • USP Type IV, Flow-Through Cell (on request)

Technical Specifications

  • Vessels: 6 or 8 borosilicate glass vessels, 1000 ml capacity
  • Temperature control: Digital, 37 degree C with accuracy of plus or minus 0.5 degree C
  • Speed range: 25 to 250 RPM (variable, digital display)
  • Basket/Paddle: SS 316 as per USP specifications
  • Timer: Programmable digital timer
  • Sampling: Manual or automatic port available
  • Compliance: USP, IP, BP, and EP pharmacopoeial standards

Regulatory Compliance

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Scientico Dissolution Apparatus meets the requirements of Pharmacy Council of India (PCI) for B.Pharm laboratory setup and is accepted for PCI inspection documentation. ISO 9001:2015 and CE certificates are provided with each unit for NAAC and accreditation purposes.

Contact: [email protected] | +91-7015865225

Experiment Guide

See the step-by-step laboratory procedure for this equipment: Dissolution Apparatus Experiment Guide, includes theory, observation table, calculations, and viva questions.

PHARMACY LAB BUYER GUIDE

Equipment mentioned in this guide

Review the product information, specifications and model before requesting a quotation.

Pharmacy Lab Equipment Manufacturer & Supplier – SCIENTICO

Pharmacy Lab Equipment Manufacturer & Supplier – SCIENTICO

SCIENTICO manufactures a complete range of pharmacy lab equipment designed for pharmacy colleges, pharmaceutical training institutes, and quality control laboratories. Our equipment supports formulation practice, dispensing training, and pharmaceutical analysis, helping students and professionals build practical skills in drug preparation and quality testing.

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Specify the dissolution method before requesting an apparatus price

A dissolution apparatus controls the movement of dosage units in a defined medium while time, temperature and sampling conditions are managed. For a teaching or quality-control requirement, the buyer should name the applicable method and dosage form, then confirm the vessel, drive, temperature-control and sampling arrangement needed for that work.

Selection pointWhat to state in the requirementWhy it matters
Apparatus methodBasket, paddle or another method required by the applicable procedureThe rotating element and setup must match the intended method.
Number of positionsTeaching demonstration, routine batch comparison or other stated workflowPosition count affects simultaneous tests, bench space and workload.
Speed controlRequired operating range, resolution, display and verification approachRotation must be set and checked against the selected procedure.
Temperature controlBath arrangement, monitoring points, display and allowed working variationMedium temperature is part of the controlled test condition.
Timing and samplingManual or supported timing, sampling points, access and sample handlingA clear sequence improves repeatability and training value.
Supplied itemsVessels, covers, shafts, baskets or paddles, probes and any toolsPrevents an apparently complete quotation from omitting required parts.
DocumentationOperating instructions, applicable calibration or verification records and offered specificationThe document set must identify the supplied configuration.

USP Apparatus 1 and Apparatus 2: the practical distinction

Apparatus 1 uses a rotating basket to contain the dosage unit. Apparatus 2 uses a paddle above the dosage unit in the vessel. The correct choice depends on the product and the procedure being followed; a purchasing page should not replace the applicable monograph, laboratory method or authorised quality instruction.

Pre-purchase laboratory checklist

  • Confirm the dosage forms and methods the laboratory intends to teach or perform.
  • Record available bench dimensions, electrical supply, water and room conditions.
  • State the number of simultaneous positions and expected daily workload.
  • Ask how speed, temperature, centring and vertical alignment are checked.
  • List every vessel, shaft, basket, paddle, cover, probe and tool required at handover.
  • Separate installation, familiarisation, calibration or verification and recurring maintenance responsibilities.
  • Require the bidder to identify deviations and optional items in the quotation.

For the operational sequence and calculation context, continue to the dissolution apparatus experiment procedure. For a broader departmental requirement, review the pharmacy laboratory equipment pathway.

RFQ wording: Provide a dissolution apparatus for the stated basket and/or paddle method. State the number of positions, speed and temperature-control arrangement, timing and sampling provisions, complete supplied accessories, utilities, documentation, installation boundary and every exclusion or optional item.
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