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FEATURED ARTICLES

  • Understanding Quality Agreements Between You And Your Contract Manufacturing Organization (CMO)
    Understanding Quality Agreements Between You And Your Contract Manufacturing Organization (CMO)

    In the broadest sense, the purpose of a quality agreement is to clearly define, establish and delineate the responsibilities of the respective QA departments from the CMO and its customer, in order to clearly communicate the responsibilities of each party, with the ultimate goal of assuring patient safety and regulatory compliance. An added benefit of implementing a clear, concise quality agreement is that it creates a more effective and efficient working relationship between CMO and customer.

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WHITE PAPERS & CASE STUDIES

  • Modular Facility Design: A Cost-Effective Option In The Post-Blockbuster Drug Era
    Modular Facility Design: A Cost-Effective Option In The Post-Blockbuster Drug Era

    The pharmaceutical industry has undergone a sea of change in recent years as manufacturers have adapted to the end of the era of large-volume production of mass-market blockbuster drugs. With firms now focusing in on subpopulations of patients, there is a need for lean, adaptable facilities that can switch quickly between multiple products in multiple formats. Modular facilities can meet this need. While not a panacea, for the right project characteristics, ‘Modularity in Design’ can deliver significant and quantifiable long-term value.

  • Fundamentals Of Spray-Dried Dispersion Technology
    Fundamentals Of Spray-Dried Dispersion Technology

    A common problem statement in the pharmaceutical industry is low oral bioavailability of drug candidates with poor aqueous solubility. The literature suggests that a significant majority of new drug candidates are in the Biopharmaceutics Classification System (BCS) class II and IV space, which includes compounds that are dissolution rate, solubility or permeability limited to absorption, or all three. As portfolios across the industry are increasingly focused on these compounds, the need for enabling technologies continues to grow.

  • Fluid Bed System Triples Batch Sizes for Laboratorios Normon while Reducing Costs
    Fluid Bed System Triples Batch Sizes for Laboratorios Normon while Reducing Costs

    With the aim of reducing costs, Normon planned to significantly increase its batch sizes for certain products. The manufacturer needed to pay close attention to the high quality and safety standards and economic aspects, as well as flexible production sizes and times.

  • Efficiencies In Powder Dispersion For Manufacturers
    Efficiencies In Powder Dispersion For Manufacturers

    This white paper explores five tips for dispersing powders into liquid more efficiently.

  • Medication Errors -- A Threat To Patient Safety: Mitigating Errors With Tablet Appearance
    Medication Errors -- A Threat To Patient Safety: Mitigating Errors With Tablet Appearance

    Medical prescription drug errors by doctors, pharmacists and patients account for 1.5 million incidences of sickness, injuries or deaths in the U.S. each year. By Jay Anbil and Steve Yoder 

  • Film Coating For Pediatric Oral Solid Dosage Forms
    Film Coating For Pediatric Oral Solid Dosage Forms

    From a recent survey conducted within the pharmaceutical industry, by Colorcon, it was confirmed that oral solid dosage forms are a preferred choice for formulation of pediatric medicines.

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PRODUCTS & SERVICES

Used Fluid Air High Shear Mixer Used Fluid Air High Shear Mixer

One (1) used Fluid Air high shear mixer, model PX1, stainless steel construction, liter bowl, 240 volt on base, serial# 10349.

Scale-Up Contract Manufacturing Services - Pharma Solid Oral Dosage Scale-Up Contract Manufacturing Services - Pharma Solid Oral Dosage

Independent of your trial size and CTM demands, Ropack Pharma Solutions is equipped to meet your needs. Using QbD principles at each phase of scale, RPS ensures that all supplies are manufactured at the highest degree of quality.

Contract Stability Testing Services - Pharma Solid Oral Dosage Contract Stability Testing Services - Pharma Solid Oral Dosage

Ropack Pharma Solutions offers ICH-compliant stability storage temperatures and, where applicable, humidity control, with many intermediate options available.

Contract Process Development - Pharma Solid Oral Dosage Contract Process Development - Pharma Solid Oral Dosage

Ropack Pharma Solutions offers fully scalable cGMP process operations from early-stage development to large-scale clinical supplies. Our experienced staff will work with you to develop a comprehensive scale-up plan with critical process parameters and QbD principles included at every manufacturing stage.

Clinical Supplies Management Services - Pharma Solid Oral Dosage Clinical Supplies Management Services - Pharma Solid Oral Dosage

Ropack Pharma Solutions welcomes the challenge of solving complex supply issues by using a unique blend of traditional and innovative services that can significantly shorten timelines, reduce cost and improve drug availability and patient compliance.

Pharmaceutical Analytical Release Services – Pharma Solid Oral Dosage Pharmaceutical Analytical Release Services – Pharma Solid Oral Dosage

Ropack Pharma Solutions’ knowledgeable staff offers a wide range of technical expertise and utilizes a diverse set of instrumentations to achieve your analytical goals. Ropack Pharma Solutions can support your product through its lifecycle from pre-IND to commercial product, including routine analysis such as CTM release and stability testing.

Contract Method Development And Transfer Services - Pharma Solid Oral Dosage Contract Method Development And Transfer Services - Pharma Solid Oral Dosage

Ropack Pharma Solution’s cGMP lab performs method development and validation for a broad spectrum of pharmaceutical compounds and dosage forms during various drug development stages.

Contract Preformulation Services - Pharma Solid Oral Dosage Contract Preformulation Services - Pharma Solid Oral Dosage

Following an agreed-upon formulation strategy, Ropack Pharma Solutions will perform preformulation studies to generate data that will lead to the key valuation milestones for your drug candidate.

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