Tachyons Lifescience Pvt. Ltd., a premier pharmaceutical manufacturing company dedicated to provide high-quality, innovative, and cost-effective solutions for the healthcare industry. With a strong commitment to excellence, we specialize in the manufacturing of Tablet, Capsules, External Preparations and Oral Liquids with assurance of the highest standards of safety, efficacy, and compliance.
We support companies by providing third party manufacturing solutions and private label solutions with the quality products so that they can concentrate on product branding and marketing. We support companies / Export house in the export business by providing quality products with the data required for registration.
TACHYONS is committed to meeting the highest international quality standards. The company has successfully undergone an EU GMP inspection conducted by the Hungary Health Authority and is currently progressing toward EU GMP certification , with authorization expected in the first quarter of 2028.
Upcoming Regulatory Inspections
These inspections further reinforce our commitment to regulatory compliance and quality excellence across international markets.
As part of our global expansion strategy, TACHYONS is preparing for regulatory inspections by the health authorities of:
Regulatory Affairs
Our dedicated Regulatory Affairs team comprises more than 20 experienced regulatory professionals with extensive expertise in managing product registrations across emerging markets, including Southeast Asia, Latin America (LATAM), the Commonwealth of Independent States (CIS), and Africa.
Our Capabilities
Preparation and submission of regulatory dossiers in Common Technical Document (CTD) format, tailored to the specific requirements of multiple emerging markets.
Strategic regulatory planning, submission management, and compliance support to ensure timely approvals and regulatory adherence.
Preparation of high-quality regulatory documentation, including:
Chemistry, Manufacturing, and Controls (CMC)
Pre-clinical documentation
Clinical documentation
Summary of Product Characteristics (SmPC/SPC)
Package Inserts (PI)
Product Labelling
Patient Information Leaflets (PIL)
Post-approval lifecycle management, including:
Market Authorization maintenance
Variation submissions
License renewals
Ongoing regulatory compliance support
Global Manufacturing Excellence
TACHYONS is a globally focused pharmaceutical manufacturer specializing in high-quality tablets, capsules, Oral Liquid and external preparation. With advanced manufacturing facilities, stringent quality systems, and a strong commitment to innovation, we offer a comprehensive portfolio of 100+ pharmaceutical products, including both generic and branded formulations.
Driven by quality, compliance, and customer trust, TACHYONS continues to expand its global footprint by delivering safe, effective, and affordable healthcare solutions to international markets.
Global Business Development
Our Presence
We have established a strong global network with business connections across 15+ countries, enabling us to support pharmaceutical companies in expanding into international markets.
Our Services
Strategic selection of target countries through a phased market expansion approach.
Country-specific regulatory guidance for product dossier preparation, submissions, registrations, and approvals.
Coordination and support for global manufacturing facility audits and regulatory inspections.
Identification and selection of the optimal product portfolio based on market demand and regulatory feasibility.
Selection, evaluation, and appointment of reliable business partners, importers, distributors, and local commercial teams.
Identification and appointment of qualified local regulatory agents in target markets.
Formulation Development
TACHYONS has extensive expertise in the development of oral solid dosage (OSD) formulations, including immediate-release, modified-release, and controlled-release dosage forms. With a strong focus on quality, efficiency, and timely project execution, we provide comprehensive formulation development services tailored to meet diverse product requirements.
Leveraging advanced technologies and scientific expertise, TACHYONS develops robust, scalable, and regulatory-compliant formulations that support successful product development from concept through commercialization.
Our formulation development capabilities include:
01
Direct Powder Blending
02
Wet & Dry Granulation
03
Tablet Compression
04
Capsule Filling
Analytical Services
TACHYONS Analytical Group brings extensive expertise in analytical method development, supported by a deep understanding of every stage of the drug development lifecycle. As your strategic development partner, we design and implement comprehensive analytical solutions tailored to your product's development phase.
Our services include the development, validation, and technology transfer of analytical methods, with detailed protocols that ensure regulatory compliance, scientific accuracy, and seamless progression from early development through commercialization. We work collaboratively to deliver reliable, high-quality analytical support that accelerates your product's journey to market.
TACHYONS Packaging team is committed to preserving the quality, potency, and safety of pharmaceutical products throughout their intended shelf life. By combining technical expertise with regulatory compliance, the team develops robust primary and secondary packaging solutions tailored to customer requirements across a wide range of solid oral dosage forms, including tablets, Capsules Oral liquid and external preparation.
The facility is equipped with advanced packaging capabilities to support diverse packaging configurations, including PVC/PVDC, Alu-Alu blister packs, HDPE bottle and laminated tube while accommodating customer- and country-specific packaging requirements. Every packaging solution is designed to ensure product integrity, regulatory compliance, and operational efficiency across global markets.
Artwork development and labelling are integral to TACHYONS packaging operations. A dedicated team manages artwork creation and lifecycle using a Right First Time approach, supported by structured project management, centralized repository management, and stringent version control systems. This ensures accuracy, traceability, and compliance with customer and regulatory expectations.
Analytical Capabilities
Analytical Method Development – Development of robust, accurate, and reproducible analytical methods for APIs, pharmaceutical formulations, and related substances.
Impurity Profiling – Identification, characterization, and quantification of process- and degradation-related impurities in accordance with regulatory guidelines.
Solubility Studies – Evaluation of drug substance and formulation solubility under various solvent systems and experimental conditions.
Dissolution Studies & Dissolution Method Development – Development, optimization, and validation of dissolution methods for solid oral dosage forms.
Multi-Media Dissolution Testing – Dissolution studies using different dissolution media to assess drug release under diverse physiological conditions.
