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Formulation Development

We develop optimal formulations by using phyto-chemicals and natural actives that have high biological effectiveness and no adverse effects for cosmeceuticals, medical devices, food supplements and OTCs.


We combine both well-known actives/herbals that are recognized by end users or health professionals and innovative substances which have been proved to be effective and safe by internationally published medical papers. By this way, the new product will easily be accepted by the target market but also have an advantage against competitors thanks to its innovative actives.


Market Analysis/Product Development
  • Market analysis for the new product.

  • Overall concept design for the product.

  • Preparing medical and marketing texts for printed or digital marketing/sales materials (catalogues, flyers etc.)

  • Customized medical sales training programs about the new product.


All these steps are planned and put into practice according to the nature of the product whether the target is end users or the health professionals. The medical educational materials are prepared and the education is given by health professionals (MD or pharmacist). After all these activities the new product will be introduced and perceived as innovative, reliable, safe and effective.


Regulatory Consulting

Long-Age is a one stop regulatory solution provider that assists their clients by getting their products registered as per and well within the expected timelines with minimal anticipated queries. Whether the product is pharmaceutical, cosmetic, medical device or food supplement, Long-Age provides flexible, end-to-end eCTD publishing services to enable companies effectively meet all their specific and unique submission requirements. Right from dossier development, planning, tracking, publishing and submitting final documents to Health Authorities Long-Age streamlines the entire Health Authority submission management process to ensure error-free, timely and quality regulatory submissions.

Clinical Trial Services
  • Design and implementation of cosmetic product clinical studies,

  • Designing of study protocols, patient registration forms, surveys, and informed consent forms,

  • Preparation, Submission and monitoring for Approval of Application Dossiers for submission to Ethics Boards-Ministry of Health

  • Arrangement of organizations or special investigational centers in clinical trials, process follow-up,

  • Calculation of sample size

  • Statistical analysis

  • Preparation of clinical study report

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