Formulation Development

Innovative Drug Delivery Methods

DRF formulation specialists develop Design of Experiments (DOE) together with risk assessment strategies using Quality-By-Design (QbD) technologies. Finding the ideal dosage form that is stable, scalable, and compliant is made possible by our development strategy, the appropriate facilities, and highly committed formulation development specialists.

1.      Pre-Factory Studies

2.      Development of Specific Formulations

3.      Development of Conventional Formulations


Wide Range Of Products

  1. NUTRACEUTICALS
  2. DIFFERENT COSMECEUTICALS FORMULATIONS
  3. PEPTIDES/PROTEINS
  4. HERBS
  5. PHYTOACTIVES
  6. SEMINAL CELLS

·         Gummies

·         Powders

·         Granules

·         Lozenges

·         Tablets

·         Capsules (Hard & Soft)

·         Pellet

·         Chocolate

·         Syrup

·         Mouth dissolving strips

·         Tea bags

·         Health drinks

·         Concentrates

·         Protein bars

·         Shampoos

·         Conditioners

·         Patches

·         Hair oils

·         Gels

Lab Scale Development To Bulk Manufacturing

  • Nanoparticles based of gold and silver
  • Lipid based nanoparticles
  • Liposomal preparation
  • Nano peptide-based delivery systems
  • Microencapsulation
  • Althea Custom formulation can be develop based on the release formats required by the client
    1. Extended
    2. Delayed
    3. Sustained

 

Location: Dixcart House, Bourne Business Park, Addlestone Rd, Addlestone KT15 2LE, UK

Comments

Post a Comment

Popular posts from this blog

Quality Assurance Healthcare

  Quality assurance in healthcare is a systematic process of monitoring, assessing, and improving the quality of healthcare services to ensure they meet established standards and deliver optimal patient outcomes. The goal of quality assurance is to enhance patient safety, effectiveness, and overall satisfaction with healthcare services. Here are key components and principles of quality assurance in healthcare: 1. Regulatory Compliance: ·   Adherence to national and international regulatory standards and guidelines is essential. Healthcare providers must ensure compliance with laws such as the Health Insurance Portability and Accountability Act (HIPAA) and follow regulations set by health authorities. 2. Clinical Guidelines and Protocols: ·    Establish and follow evidence-based clinical guidelines and protocols to standardize care processes. This helps ensure that healthcare practices are based on the latest research and best practices. 3. Continuous Qu...
Read more

Clinical Services

Clinical services in the context of drug development refer to the activities and studies conducted during the clinical trial phase of drug testing, involving human subjects. Clinical services encompass a range of trials, including early-phase (Phase I), middle-phase (Phase II), and late-phase (Phase III) trials. Here are key components of clinical services: Clinical Trial Design: Develop the overall plan for the clinical trial, including the study objectives, patient population, study duration, and endpoints. Clinical Site Selection: Identify and choose suitable locations (sites) where the clinical trials will be conducted. Patient Recruitment and Enrollment: Recruit eligible participants according to the study criteria and ensure their informed consent before enrollment. Clinical Trial Monitoring: Oversee and supervise the progress of the clinical trial at various sites to ensure compliance with the protocol and regulatory requirements. Clinical Data Management: Collect, proces...
Read more