Tired of coordinating formulator, manufacturer, packaging and customs separately?

ASPharma operates as a single accountable partner, handling the entire process from formulation to final delivery under one roof. You get one point of contact and simpler coordination, without having to manage multiple suppliers.

The cost depends on formulation complexity, production volume, and required services. We offer personalized quotes with no commitment.

Yes. ASPharma can evaluate low-volume projects or pilot batches, provided they are viable based on the type of product, format, total volume, and manufacturing or import conditions. Our approach is to review each case individually to find a solution that lets you validate the product in the market without compromising quality, regulatory compliance, or the project's profitability.

The typical timeline is 10-14 weeks from formula approval to finished product delivery. This includes formula development (2-4 weeks), sourcing (1-2 weeks), production (3-4 weeks), packaging (1-2 weeks), and logistics (2-3 weeks).

Yes. We develop organic, vegan, kosher and free-from formulations according to each client’s technical, regulatory and commercial requirements.

• Formulations with certified organic ingredients, subject to availability and target market
• Vegan / plant-based products with documented raw-material backing
• Coordination of kosher certifications with certifying bodies
• Free-from claims: gluten-free, dairy-free, soy-free, among others
• Clean label development with natural ingredients and technical traceability

We implement a multi-stage quality control system: supplier and ingredient validation, in-process inspections during production, independent third-party lab testing (SGS) and final verification before shipping. All our production partners maintain active ISO, FDA and GMP certifications.

The required documents depend on the product category and the applicable health regulations. In general, these may include quality certificates, GMP certifications, technical data sheets, formulas or compositions, free-sale certificates, labeling compliant with Chilean regulations, sanitary registrations or authorizations, and import permits from the relevant authority.

ASPharma assesses each case according to the type of product (supplements, cosmetics, medical devices, medicines or other regulated products) and manages the documentation needed to meet the requirements of the ISP, SEREMI de Salud, Customs and other competent bodies.

ASPharma reviews the technical, sanitary and quality documentation of each product and ingredient, including certificates of analysis, technical sheets, composition, labeling, origin and manufacturer background, according to the corresponding regulatory category.

This review makes it possible to assess traceability, documentary backing and regulatory compliance before starting import, registration, notification or commercialization processes in Chile.

Yes. ASPharma works with a wide range of clients and commercial channels, including gyms, pharmacies, e-commerce, specialized stores, distributors, importers, entrepreneurs, clinics and health professionals. We support private-label brand development.