In today’s competitive pharmaceutical landscape, meeting regulatory standards is just the starting point — true differentiation comes from delivering tablets that consistently demonstrate purity, potency, and efficacy. At Cohiba Pharma, we take this responsibility seriously. From sourcing raw materials to final release testing, we have built robust processes that ensure each tablet batch lives up to our high standards. In this article, we walk you through the key pillars of our quality programme, and show how Cohiba Pharma sets the benchmark for tablet formulation.

Table of Contents

1. Premium Raw Material Sourcing & Supplier Qualification

The journey to a high-quality tablet begins well before manufacturing — it begins with the active pharmaceutical ingredients (APIs), excipients and packaging components. At Cohiba Pharma, we only partner with suppliers who meet stringent qualification criteria: certificate of analysis (CoA), audit evidence, and track record of compliance. Our manufacturing premises are described as “state-of-the-art internationally approved” which underscores our commitment to quality.
By controlling this first step, we guard against contamination, degradation and variability that could compromise tablet performance.

2. Modern WHO-GMP Facilities & Manufacturing Controls

Once materials arrive, the manufacturing process takes place in our WHO-GMP-compliant facilities. Cohiba Pharma has emphasised that its operations are carried out in “state‐of‐the‐art internationally approved manufacturing premises” where “all the molecules are clinically tested and prepared” under rigorous conditions.

Key controls include:

Dedicated suites for tablet formulation and coating, with controlled temperature, humidity, and airflow.
Automated weighing and dispensing of APIs and excipients to minimise human error.
In-process monitoring of tablet weight, hardness, friability, disintegration time, and other critical parameters.

These systems ensure that the tablets you receive match their intended design and deliver the expected dosage.

3. Stringent Quality Control & Analytical Testing

After manufacturing, the tablet batches undergo a battery of quality checks to confirm purity, potency and stability. Cohiba Pharma’s product listing emphasises the company’s focus on quality: “Trusted for their purity, efficacy, and safety.”
Some of the analytical procedures include:

Assay testing: Confirming that each tablet contains the correct quantity of API.
Impurity/purity profiling: Detecting and quantifying any related substances, degradants of unreacted starting materials.
Dissolution testing: Ensuring the tablet releases its actives at the right rate and extent — critical for efficacy.
Stability testing: Simulating storage over time to verify that potency and integrity remain intact under varied conditions (heat, humidity, light).
Such rigorous testing ensures that every tablet meets engineered specifications and regulatory requirements before being released to the market.

4. Regulatory Compliance & Certification

Adherence to regulatory frameworks is fundamental. Cohiba Pharma’s operations emphasise compliance with national and international quality standards. Their product information mentions capsules and tablets manufactured under WHO-GMP (Good Manufacturing Practices) and other recognized systems.
By maintaining such certifications and regulatory alignment, Cohiba Pharma ensures that its tablets are not only safe and effective for the Indian market, but also meet global benchmarks where applicable.

5. Robust Packaging & Storage to Preserve Efficacy

Even the best-manufactured tablet can lose potency or suffer degradation if packaging or storage is inadequate. Cohiba Pharma pays attention to this stage. Tablets are packed in moisture- and light-barrier packaging (blister, aluminium-foil, PVC etc as appropriate), clearly labelled, and stored in controlled warehousing until dispatch. Proper logistics ensure that tablets arrive at pharmacies or end-users under optimal conditions, preserving efficacy.

6. Continuous Improvement & Innovation

Quality is not a static endpoint — it is a continuous journey. At Cohiba Pharma, processes are continually reviewed and refined. Manufacturing data, customer feedback and post-market surveillance feed into improvement loops. New formulation technologies, better coatings, improved excipient selections and more sophisticated analytics are all part of our drive to raise the bar. This mindset ensures that the tablets you trust today will stay reliable tomorrow.

7. Why Purity and Efficacy Matter for Patients & Stakeholders

For patients, the implications of purity and efficacy are clear — an impure tablet can mean unexpected side-effects or reduced therapeutic benefit; an inefficient formulation can mean slower onset or incomplete relief. For pharmacists, physicians, and business-partners, having a manufacturing partner like Cohiba Pharma gives assurance that the products on the shelf truly perform. In short, a tablet that fails to meet quality expectations costs far more than lower regulatory fees — it undermines trust. By maintaining excellence, Cohiba Pharma protects patient safety, strengthens brand reputation, and supports healthcare outcomes.

8. Conclusion

In the realm of pharmaceuticals, formulation quality is foundational. At Cohiba Pharma, our commitment to purity and efficacy of tablet formulations is woven into every stage of the value chain — from raw-material sourcing to finished-product release and beyond. If you’re seeking a partner or a product line that stands up to the most demanding quality requirements, look to Cohiba Pharma. With robust processes, modern facilities, rigorous testing and a mindset of continuous improvement, we deliver tablet formulations you can trust.

For more details about our tablet range or partnership opportunities, visit cohibapharma.com and explore our product portfolio.
Thank you for trusting Cohiba Pharma — where quality, safety and efficacy come together.

How Cohiba Pharma Ensures the Purity and Efficacy of Its Tablet Formulations