Emerging trends in pharma formulation development
November 27, 2025
|Chronicle Pharmabiz
We, the Indian pharma industry stands at the beginning of a transformative era.
Already earned global recognition as the “Pharmacy of the World” for its dominance in the generics market, India is now moving towards innovation-driven growth, a long pending one.
The U.S. share (>40% of generic prescriptions, see Table 1) underlines how dependent key regulated markets are on Indian manufacturers. The focus is shifting from replicating existing formulations to creating novel, patient-centric, individualized, cost- effective and technology-enabled drug delivery systems.
The next phase of progress in Indian pharma lies in advancing drug formulation -from the development of Novel Drug Delivery Systems (NDDS) to the exploration of 3D printing technologies and personalized medicines.This technology not only increases therapeutic efficacy and patient compliance but also align with the evolving expectations of global healthcare systems that emphasize precision, sustainability, and accessibility.
NDDS redefining therapeutic efficiency
The concept of NDDS in India has evolved markedly from simple controlled-release tablets to highly advanced systems such as nanoparticles, liposomes, niosomes, phytosomes, microspheres, and transdermal patches. The goal of NDDS is not merely to improve bioavailability but to achieve targeted, sustained, and safer drug delivery.
From conventional to advanced systems
India's initial NDDS efforts focused on oral sustained-release systems in the 1990s. Gradually, Indian scientists and formulators embraced polymeric systems, osmotic pumps, and mucoadhesive technologies. Today, the emphasis has expanded toward nanotechnology-based systems such as:
- Liposomal and niosomal carriers (e.g., Amphotericin B liposomes),
- Polymeric nanoparticles for anticancer and antiviral agents,
هذه القصة من طبعة November 27, 2025 من Chronicle Pharmabiz.
اشترك في Magzter GOLD للوصول إلى آلاف القصص المتميزة المنسقة، وأكثر من 9000 مجلة وصحيفة.
هل أنت مشترك بالفعل؟ تسجيل الدخول
المزيد من القصص من Chronicle Pharmabiz
Chronicle Pharmabiz
US FDA fortifies alliance with Telangana DCA
A high-level delegation from the US FDA concluded a significant meeting with the DCA in Telangana, two days ago, at the DCA office in Hyderabad.
2 mins
December 11, 2025
Chronicle Pharmabiz
India exploring possibilities to expand WHO standards for Indian medicines
INDIA is looking at possibilities to expand the World Health Organisation (WHO) global benchmarking standards for medicines, in order to unify and strengthen the drug regulatory mechanism for safety, quality and efficacy of medicines sold in the country.
1 min
December 11, 2025
Chronicle Pharmabiz
Eli Lilly gets US FDA approval for Jaypirca
Eli Lilly and Company announced that the US Food and Drug Administration (FDA) has granted approval to Jaypirca (pirtobrutinib, 100 mg & 50 mg tablets) for the treatment of adults with relapsed or refractory chronic lymphocytic leukaemia or small lymphocytic lymphoma (CLL/SLL) who have previously been treated with a covalent Bruton tyrosine kinase (BTK) inhibitor.
1 mins
December 11, 2025
Chronicle Pharmabiz
Haryana DCA focuses on quality overhaul
THE Haryana drug control administration (DCA) is undertaking a major organizational overhaul focused on quality system upgrades and regulatory capacity building, particularly in response to the revised Schedule M norms.
2 mins
December 11, 2025
Chronicle Pharmabiz
DoC seeks inputs on trade issues faced with Japan
THE Department of Commerce (DoC), under the Union Commerce Ministry, has sought inputs from the industry on specific issues being faced in pharma trade with Japan.
1 min
December 11, 2025
Chronicle Pharmabiz
AIOCD asks traders to strictly comply with ban on 35 FDCs
THE All India Organisation of Chemists and Druggists (AIOCD) has issued an urgent internal circular to all its state and Union territory trade bodies, demanding immediate and strict compliance with the ban on 35 fixed dose combinations (FDCs).
3 mins
December 11, 2025
Chronicle Pharmabiz
US FDA approves Bristol Myers Squibb's Breyanzi
Bristol Myers Squibb announced that the US Food and Drug Administration (FDA) has granted approval of Breyanzi (lisocabtagene maraleucel; liso-cel), a CD19-directed chimeric antigen receptor (CAR) T cell therapy, for the treatment of adult patients with relapsed or refractory (R/R) marginal zone lymphoma (MZL) who have received at least two prior lines of systemic therapy.
2 mins
December 11, 2025
Chronicle Pharmabiz
CN Water presents AQU@Sense MB
CN Water is now combining core water-system expertise with digital assurance has launched AQU@Sense which delivers microbial test results in under 30 minutes, replacing traditional 5 to 7 days culture based methods.
1 min
December 11, 2025
Chronicle Pharmabiz
Pharma logistics sees policy push as key catalyst for growth
INDIAN pharma's logistics sector is getting major boost from emerging policy support.
2 mins
December 11, 2025
Chronicle Pharmabiz
Lack of financial aid, expertise mar MSME prospects to meet revised Sch M deadline
INDUSTRY experts have raised alarm that lack of financial assistance and guidance on technical expertise have marred pharma MSMEs’ prospects to comply with revised Schedule M guidelines of December 31, 2025.
2 mins
December 11, 2025
Listen
Translate
Change font size

